Probe set ID	Variability score	Variability rank	Mean	Standard Deviation	Present regions	Symbol	Name	Gene Category
13701	1449341_a_at	-0.274547	13796	8.57252	0.201272	7	Stom	stomatin
13702	1453819_x_at	-0.208339	12851	8.57272	0.215249	2	Stx18	syntaxin 18
13703	1418073_at	0.0759528	8566	8.57329	0.285761	48	Acot9	acyl-CoA thioesterase 9
13704	1457252_x_at	0.218979	6599	8.5737	0.330007	37	Pld2	phospholipase D2
13705	1420863_at	0.294898	5731	8.57389	0.356037	48	Dctn4	dynactin 4
13706	1450824_at	0.141363	7618	8.57415	0.305362	3	Ptch1	patched homolog 1
13707	1429541_at	-0.54349	16838	8.57425	0.154052	45	Zfp777	zinc finger protein 777
13708	1441114_at	0.317333	5480	8.5744	0.364349	48	9330156P08Rik	RIKEN cDNA 9330156P08 gene
13709	1433600_at	1.32847	291	8.57478	1.0015	46	Adra2a	adrenergic receptor, alpha 2a	GPCR NH/NT
13710	1452788_at	0.100838	8183	8.57498	0.293235	48	Ppp2r5e	protein phosphatase 2, regulatory subunit B (B56), epsilon isoform
13711	1441047_at	0.176821	7139	8.57521	0.316588	48	Slc45a4	solute carrier family 45, member 4
13712	1432249_a_at	-0.3875	15252	8.57533	0.179942	38	Ercc8	excision repaiross-complementing rodent repair deficiency, complementation group 8
13713	1435981_at	0.47036	3970	8.57569	0.423928	48	Nav2	neuron navigator 2
13714	1423926_at	-0.604301	17328	8.57602	0.144735	27	Slc39a13	solute carrier family 39 (metal ion transporter), member 13
13715	1433473_x_at	-0.686723	17818	8.57607	0.133408	48	Tm2d2	TM2 domain containing 2
13716	1448665_at	0.353324	5100	8.57629	0.377458	48	Dmd	dystrophin, muscular dystrophy	EM SP
13717	1440259_at	0.304214	5622	8.57663	0.359369	23
13718	1460386_a_at	0.797768	1798	8.5769	0.588144	33	Slc1a1	solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1	SLC
13719	1417100_at	-0.48034	16248	8.5769	0.163836	34	Cd320	CD320 antigen
13720	1434258_s_at	0.0796898	8499	8.57691	0.286831	36	Phactr4	phosphatase and actin regulator 4
13721	1421797_a_at	-0.229385	13150	8.57741	0.21057	27	Snx12	sorting nexin 12
13722	1446288_at	-0.378575	15143	8.57746	0.181386	48	C78692	expressed sequence C78692
13723	1424559_at	-0.121009	11575	8.57768	0.234892	48	Rpap2	RNA polymerase II associated protein 2
13724	1437910_at	-0.260816	13618	8.57773	0.204377	48	Tmem39b	transmembrane protein 39b
13725	1418359_at	-0.148154	11969	8.57776	0.228781	2	Wbscr27	Williams Beuren syndrome chromosome region 27 (human)

TF=Transcription Factor; Ch=Channel; GPCR=GPCR; CA=Cell Adhesion; EM=Extracellular Matrix; SP=Structural Protein; Ng=Neurogenesis; Hox=Homeobox; NR=Nuclear Receptor; NH/NT=NH/NT; AG=Axon Guidance; SLC=SLC Transporter; Fox=Forkhead