Variant report

Variant	rs3740512
Chromosome Location	chr10:99078745-99078746
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBP	chr10:99078511-99079234	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr10:99078576-99079167	HepG2	liver:	n/a	chr10:99079037-99079053 chr10:99079029-99079045
3	MXI1	chr10:99078510-99079361	GM12878	blood:	n/a	n/a
4	ZBTB7A	chr10:99078414-99079316	ECC-1	luminal epithelium:	n/a	n/a
5	POLR2A	chr10:99078490-99080301	NB4	blood:	n/a	n/a
6	POLR2A	chr10:99078455-99079309	HepG2	liver:	n/a	n/a
7	RCOR1	chr10:99078732-99078914	K562	blood:	n/a	n/a
8	JUND	chr10:99078685-99079182	HepG2	liver:	n/a	chr10:99078982-99078991
9	POLR2A	chr10:99078682-99079654	MCF-7	breast:	n/a	n/a
10	PAX5	chr10:99078563-99079102	GM12878	blood:	n/a	n/a
11	MXI1	chr10:99078571-99079263	H1-hESC	embryonic stem cell:	n/a	n/a
12	EP300	chr10:99078419-99079311	ECC-1	luminal epithelium:	n/a	n/a
13	MAZ	chr10:99078598-99079283	Hela-S3	cervix:	n/a	n/a
14	CTBP2	chr10:99078664-99079475	H1-hESC	embryonic stem cell:	n/a	n/a
15	ZMIZ1	chr10:99078733-99079095	K562	blood:	n/a	n/a
16	ARID3A	chr10:99078685-99079065	K562	blood:	n/a	n/a
17	FOS	chr10:99078686-99079069	MCF10A-Er-Src	breast:	n/a	chr10:99078982-99078991
18	POLR2A	chr10:99078444-99079692	K562	blood:	n/a	n/a
19	MAX	chr10:99078490-99079638	K562	blood:	n/a	n/a
20	ZNF143	chr10:99078743-99079133	H1-hESC	embryonic stem cell:	n/a	n/a
21	HEY1	chr10:99078495-99079553	HepG2	liver:	n/a	chr10:99078983-99078992 chr10:99079039-99079054 chr10:99078981-99078990 chr10:99079036-99079051
22	SP1	chr10:99078515-99079244	A549	lung:	n/a	chr10:99078952-99078961
23	ATF2	chr10:99078393-99079195	H1-hESC	embryonic stem cell:	n/a	chr10:99078981-99078992
24	TBL1XR1	chr10:99078579-99079130	K562	blood:	n/a	n/a
25	FOXA2	chr10:99078414-99079361	HepG2	liver:	n/a	n/a
26	FOXM1	chr10:99078559-99079192	GM12878	blood:	n/a	n/a
27	POLR2A	chr10:99078452-99079514	K562	blood:	n/a	n/a
28	POLR2A	chr10:99078728-99079453	GM15510	blood:	n/a	n/a
29	TCF12	chr10:99078507-99079108	H1-hESC	embryonic stem cell:	n/a	chr10:99078996-99079005
30	ELK1	chr10:99078560-99079124	Hela-S3	cervix:	n/a	n/a
31	EGR1	chr10:99078516-99079147	ECC-1	luminal epithelium:	n/a	chr10:99078714-99078728
32	E2F6	chr10:99078480-99079896	K562	blood:	n/a	chr10:99078983-99078992 chr10:99078981-99078990
33	IRF4	chr10:99078652-99079019	GM12878	blood:	n/a	n/a
34	NFIC	chr10:99078558-99079110	GM12878	blood:	n/a	n/a
35	TBL1XR1	chr10:99078591-99079016	GM12878	blood:	n/a	n/a
36	SIN3AK20	chr10:99078385-99080207	PANC-1	pancreas:	n/a	n/a
37	TEAD4	chr10:99078479-99079295	ECC-1	luminal epithelium:	n/a	n/a
38	EGR1	chr10:99078514-99079090	K562	blood:	n/a	chr10:99078714-99078728
39	TCF7L2	chr10:99078589-99079150	Hela-S3	cervix:	n/a	n/a
40	ATF3	chr10:99078639-99079083	A549	lung:	n/a	chr10:99078980-99078993 chr10:99078983-99078994 chr10:99078982-99078993 chr10:99078982-99078990 chr10:99078981-99078992 chr10:99078980-99078993 chr10:99078983-99078991 chr10:99078979-99078992 chr10:99078983-99078990 chr10:99078980-99078990 chr10:99078981-99078992 chr10:99078979-99078994
41	POLR2A	chr10:99078575-99079382	HEK293	kidney:	n/a	n/a
42	TCF12	chr10:99078394-99079415	ECC-1	luminal epithelium:	n/a	chr10:99078996-99079005
43	MAX	chr10:99078405-99079803	K562	blood:	n/a	n/a
44	SIX5	chr10:99078313-99079152	A549	lung:	n/a	chr10:99078601-99078610
45	FOXA1	chr10:99078594-99079147	ECC-1	luminal epithelium:	n/a	n/a
46	EGR1	chr10:99078466-99079018	MCF-7	breast:	n/a	chr10:99078714-99078728
47	HEY1	chr10:99078503-99078758	K562	blood:	n/a	n/a
48	BHLHE40	chr10:99078525-99079243	K562	blood:	n/a	chr10:99079037-99079053 chr10:99079029-99079045
49	SIN3A	chr10:99078476-99080543	H1-hESC	embryonic stem cell:	n/a	chr10:99079177-99079190 chr10:99079183-99079191
50	SP1	chr10:99078415-99079298	A549	lung:	n/a	chr10:99078952-99078961

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99078702-99078752	T-47D	breast:	n/a
2	chr10:99078702-99078752	HCM	heart:	n/a
3	chr10:99078702-99078752	Hepatocyte	liver:	n/a
4	chr10:99078702-99078752	AG09319	gingival:	n/a
5	chr10:99078702-99078752	HEEpiC	esophagus:	n/a
6	chr10:99078702-99078752	HEK293	kidney:	embryo
7	chr10:99078702-99078752	HCF	heart:	n/a
8	chr10:99078702-99078752	HL-60	blood:	n/a
9	chr10:99078702-99078752	MCF10A-Er-Src	breast:	n/a
10	chr10:99078702-99078752	HUVEC	blood vessel:	n/a
11	chr10:99078702-99078752	Caco-2	colon:	n/a
12	chr10:99078702-99078752	HepG2	liver:	n/a
13	chr10:99078702-99078752	GM12891	blood:	n/a
14	chr10:99078702-99078752	HAEpiC	amniotic membrane:	n/a
15	chr10:99078702-99078752	K562	blood:	n/a
16	chr10:99078702-99078752	U87	brain:	n/a
17	chr10:99078702-99078752	GM12892	blood:	n/a
18	chr10:99078702-99078752	NH-A	brain:	n/a
19	chr10:99078702-99078752	SAEC	small airway:	n/a
20	chr10:99078702-99078752	NHBE	bronchial:	n/a
21	chr10:99078702-99078752	GM06990	blood:	n/a
22	chr10:99078702-99078752	SK-N-MC	brain:	n/a
23	chr10:99078702-99078752	AG09309	skin:	n/a
24	chr10:99078702-99078752	A549	lung:	n/a
25	chr10:99078702-99078752	HRPEpiC	eye:	n/a
26	chr10:99078702-99078752	NHDF-neo	bronchial:	n/a
27	chr10:99078702-99078752	HIPEpiC	eye:	n/a
28	chr10:99078702-99078752	HCT-116	colon:	n/a
29	chr10:99078702-99078752	LNCaP	prostate:	n/a
30	chr10:99078702-99078752	IMR90	lung:	fetal
31	chr10:99078702-99078752	SK-N-SH	brain:	n/a
32	chr10:99078702-99078752	MCF-7	breast:	n/a
33	chr10:99078702-99078752	RPTEC	kidney:	n/a
34	chr10:99078702-99078752	GM12878	blood:	n/a
35	chr10:99078702-99078752	HPAEpiC	pulmonary alveolar:	n/a
36	chr10:99078702-99078752	CMK	blood:	n/a
37	chr10:99078702-99078752	ovcar-3	ovarian:	n/a
38	chr10:99078702-99078752	Hela-S3	cervix:	n/a
39	chr10:99078702-99078752	BE2_C	brain:	n/a
40	chr10:99078702-99078752	GM19239	blood:	n/a
41	chr10:99078702-99078752	H1-hESC	embryonic stem cell:	embryo
42	chr10:99078702-99078752	HRCEpiC	kidney:	n/a
43	chr10:99078702-99078752	HCPEpiC	choroid plexus:	n/a
44	chr10:99078702-99078752	HRE	kidney:	n/a
45	chr10:99078702-99078752	NT2-D1	testis:	n/a
46	chr10:99078702-99078752	Jurkat	blood:	n/a
47	chr10:99078702-99078752	AoSMC	blood vessel:	n/a
48	chr10:99078702-99078752	AG04450	lung:	fetal
49	chr10:99078702-99078752	ECC-1	luminal epithelium:	n/a
50	chr10:99078702-99078752	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:99051058..99054984-chr10:99078319..99082092,7	MCF-7	breast:
2	chr10:99078612..99079288-chr16:20752504..20753231,2	Hela-S3	cervix:
3	chr1:145382532..145383482-chr10:99078590..99079115,2	Hela-S3	cervix:
4	chr10:99078212..99079127-chr2:113342181..113342990,2	Hela-S3	cervix:
5	chr10:99050343..99055587-chr10:99077475..99082102,7	MCF-7	breast:
6	chr10:99051582..99054067-chr10:99077169..99079188,3	K562	blood:
7	chr10:99051582..99055310-chr10:99077169..99083058,6	K562	blood:
8	chr1:234746282..234747092-chr10:99078304..99078804,2	Hela-S3	cervix:
9	chr10:99066690..99071389-chr10:99076606..99080814,5	MCF-7	breast:

Variant related genes	Relation type
FRAT1	TF binding region
FRAT1	CpG island
ENSG00000201558	Chromatin interaction
ENSG00000269891	Chromatin interaction
ENSG00000125611	Chromatin interaction
ENSG00000213390	Chromatin interaction
ENSG00000066654	Chromatin interaction
ENSG00000237169	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10736115	0.87[CEU][hapmap];0.81[GIH][hapmap];0.81[JPT][hapmap];0.81[MEX][hapmap];0.86[TSI][hapmap]
rs10736116	0.86[EUR][1000 genomes]
rs10748691	0.96[CEU][hapmap];0.80[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap]
rs10748692	0.81[EUR][1000 genomes]
rs10748694	0.96[CEU][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10786321	0.87[CEU][hapmap];0.81[JPT][hapmap];0.81[MEX][hapmap];0.86[TSI][hapmap]
rs10786324	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10786325	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10786326	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10786327	0.82[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10786329	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10786330	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10786332	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10786333	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10786334	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10786335	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882881	0.96[CEU][hapmap];0.80[JPT][hapmap]
rs10882883	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs10882884	0.95[CEU][hapmap];0.85[JPT][hapmap];0.83[EUR][1000 genomes]
rs10882889	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10882891	0.95[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10882894	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10882895	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10882897	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10882898	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10882899	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11189100	0.83[EUR][1000 genomes]
rs11189120	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11189122	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11189127	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11189131	0.91[TSI][hapmap];0.90[EUR][1000 genomes]
rs11189132	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11189137	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11189138	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12221430	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12413688	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12571098	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1334892	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1468069	0.91[CEU][hapmap]
rs1890966	0.98[ASN][1000 genomes]
rs2065861	0.85[CEU][hapmap]
rs2297987	0.91[CEU][hapmap];0.80[JPT][hapmap]
rs2861875	0.96[CEU][hapmap];0.80[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap]
rs3740522	0.96[CEU][hapmap];0.80[GIH][hapmap];0.85[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs3781373	0.91[CEU][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3814164	0.96[CEU][hapmap];0.80[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap]
rs4917766	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4919087	0.82[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4919089	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4919090	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4919091	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61863767	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6584116	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7067835	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7072078	0.83[EUR][1000 genomes]
rs7076523	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7078288	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.95[TSI][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7080275	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7089634	0.81[EUR][1000 genomes]
rs7901853	0.87[CEU][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs945187	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs945189	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532232	chr10:98360775-99141797	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1041614	chr10:98928281-99083056	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv1045553	chr10:98944397-99122203	Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv540750	chr10:98944397-99122203	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv831952	chr10:98998344-99145924	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv895914	chr10:99006083-99131676	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv825533	chr10:99070570-99115599	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	esv3375506	chr10:99078187-99080735	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv3345502	chr10:99078562-99080560	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	esv3358377	chr10:99078587-99081135	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3740512	EXOSC1	cis	parietal	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99077600-99079800	Active TSS	Fetal Intestine Large	intestine
2	chr10:99077600-99079800	Active TSS	Hela-S3	cervix
3	chr10:99077600-99080200	Active TSS	Brain Hippocampus Middle	brain
4	chr10:99077800-99080000	Active TSS	Primary T cells from cord blood	blood
5	chr10:99078000-99078800	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr10:99078000-99079600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr10:99078000-99081200	Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr10:99078000-99081400	Active TSS	Monocytes-CD14+_RO01746	blood
9	chr10:99078200-99078800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:99078200-99078800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr10:99078200-99079400	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
12	chr10:99078200-99079400	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
13	chr10:99078200-99079600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:99078200-99079600	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr10:99078200-99079600	Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr10:99078200-99079600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:99078200-99079600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:99078200-99079600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:99078200-99079600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr10:99078200-99079600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:99078200-99079600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr10:99078200-99079600	Active TSS	Fetal Brain Female	brain
23	chr10:99078200-99079600	Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr10:99078200-99079800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr10:99078200-99079800	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr10:99078200-99079800	Active TSS	Muscle Satellite Cultured Cells	--
27	chr10:99078200-99079800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr10:99078200-99079800	Active TSS	Fetal Intestine Small	intestine
29	chr10:99078200-99079800	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr10:99078200-99080000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:99078200-99080000	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr10:99078200-99080000	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr10:99078200-99080000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
34	chr10:99078200-99080000	Active TSS	Brain Anterior Caudate	brain
35	chr10:99078200-99080000	Active TSS	Brain Cingulate Gyrus	brain
36	chr10:99078200-99080000	Active TSS	Brain Substantia Nigra	brain
37	chr10:99078200-99080000	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr10:99078200-99080200	Active TSS	H9 Cell Line	embryonic stem cell
39	chr10:99078200-99080200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
40	chr10:99078200-99080200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
41	chr10:99078200-99080200	Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr10:99078200-99080200	Active TSS	Brain Inferior Temporal Lobe	brain
43	chr10:99078200-99080200	Active TSS	Duodenum Mucosa	Duodenum
44	chr10:99078200-99080200	Active TSS	Fetal Kidney	kidney
45	chr10:99078200-99080200	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr10:99078200-99080200	Active TSS	Thymus	Thymus
47	chr10:99078200-99081000	Active TSS	Psoas Muscle	Psoas
48	chr10:99078200-99081200	Active TSS	Brain Angular Gyrus	brain
49	chr10:99078200-99081200	Active TSS	Colon Smooth Muscle	Colon
50	chr10:99078200-99081200	Active TSS	Pancreatic Islets	Pancreatic Islet

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