Variant report

Variant	rs9263786
Chromosome Location	chr6:31126230-31126231
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	BRCA1	chr6:31125686-31126511	Hela-S3	cervix:	n/a	n/a
2	ZKSCAN1	chr6:31126047-31126550	Hela-S3	cervix:	n/a	n/a
3	E2F6	chr6:31125886-31126554	A549	lung:	n/a	chr6:31126205-31126217 chr6:31126020-31126029 chr6:31126234-31126249 chr6:31125904-31125916 chr6:31126279-31126288 chr6:31126085-31126094
4	CHD2	chr6:31125857-31126525	Hela-S3	cervix:	n/a	n/a
5	MAX	chr6:31125693-31126610	A549	lung:	n/a	n/a
6	SP2	chr6:31125935-31126472	H1-hESC	embryonic stem cell:	n/a	chr6:31126274-31126289
7	PML	chr6:31126134-31126648	K562	blood:	n/a	chr6:31126591-31126599
8	STAT3	chr6:31126046-31126254	MCF10A-Er-Src	breast:	n/a	n/a
9	POLR2A	chr6:31125765-31126531	HUVEC	blood vessel:	n/a	n/a
10	SP1	chr6:31125873-31126579	GM12878	blood:	n/a	chr6:31126258-31126279 chr6:31125998-31126010 chr6:31125973-31125983 chr6:31125906-31125920 chr6:31125973-31125983 chr6:31125998-31126010 chr6:31126278-31126290 chr6:31126280-31126289 chr6:31125999-31126008 chr6:31126278-31126290 chr6:31126062-31126076 chr6:31125907-31125916 chr6:31126279-31126288 chr6:31125896-31125910 chr6:31126204-31126215
11	E2F6	chr6:31125936-31126307	K562	blood:	n/a	chr6:31126205-31126217 chr6:31126020-31126029 chr6:31126234-31126249 chr6:31126279-31126288 chr6:31126085-31126094
12	EGR1	chr6:31125874-31126598	MCF-7	breast:	n/a	chr6:31125908-31125921 chr6:31126274-31126287 chr6:31126275-31126289 chr6:31126020-31126029 chr6:31126085-31126094 chr6:31126274-31126287 chr6:31126277-31126286
13	YY1	chr6:31126144-31126566	GM12878	blood:	n/a	chr6:31126513-31126524
14	HNF4G	chr6:31126005-31126509	HepG2	liver:	n/a	n/a
15	E2F1	chr6:31125932-31126589	Hela-S3	cervix:	n/a	chr6:31126205-31126217 chr6:31126020-31126029 chr6:31126234-31126249 chr6:31126279-31126288 chr6:31126085-31126094
16	MAX	chr6:31125928-31126803	Hela-S3	cervix:	n/a	n/a
17	GABPA	chr6:31125991-31126561	K562	blood:	n/a	chr6:31126021-31126030 chr6:31126084-31126098 chr6:31126019-31126033 chr6:31126084-31126095 chr6:31126016-31126030 chr6:31126019-31126030 chr6:31126081-31126095
18	POLR2A	chr6:31125634-31126773	U87	brain:	n/a	n/a
19	POLR2A	chr6:31125773-31126606	A549	lung:	n/a	n/a
20	MAX	chr6:31125993-31126620	SK-N-SH	brain:	n/a	n/a
21	SP1	chr6:31125937-31126526	H1-hESC	embryonic stem cell:	n/a	chr6:31126258-31126279 chr6:31125998-31126010 chr6:31125973-31125983 chr6:31125973-31125983 chr6:31125998-31126010 chr6:31126278-31126290 chr6:31126280-31126289 chr6:31125999-31126008 chr6:31126278-31126290 chr6:31126062-31126076 chr6:31126279-31126288 chr6:31126204-31126215
22	ELF1	chr6:31125937-31126576	MCF-7	breast:	n/a	chr6:31126348-31126360 chr6:31125993-31126005 chr6:31125999-31126011
23	SP2	chr6:31125841-31126562	HepG2	liver:	n/a	chr6:31126274-31126289
24	POLR2A	chr6:31126187-31126861	GM12891	blood:	n/a	n/a
25	POLR2A	chr6:31126214-31126598	GM12878	blood:	n/a	n/a
26	POLR2A	chr6:31125744-31126525	NB4	blood:	n/a	n/a
27	CHD2	chr6:31125792-31126510	K562	blood:	n/a	n/a
28	POLR2A	chr6:31125669-31126501	HCT-116	colon:	n/a	n/a
29	HNF4A	chr6:31126033-31126480	HepG2	liver:	n/a	n/a
30	YY1	chr6:31126157-31126568	GM12892	blood:	n/a	chr6:31126513-31126524
31	SP2	chr6:31126003-31126415	K562	blood:	n/a	chr6:31126274-31126289
32	EGR1	chr6:31126024-31126475	K562	blood:	n/a	chr6:31126274-31126287 chr6:31126275-31126289 chr6:31126085-31126094 chr6:31126274-31126287 chr6:31126277-31126286
33	POLR2A	chr6:31125539-31127594	HepG2	liver:	n/a	n/a
34	MAX	chr6:31126067-31126532	K562	blood:	n/a	n/a
35	THAP1	chr6:31125994-31126530	K562	blood:	n/a	n/a
36	MAFK	chr6:31126098-31126344	HepG2	liver:	n/a	n/a
37	NFYB	chr6:31125939-31126832	Hela-S3	cervix:	n/a	chr6:31126259-31126269 chr6:31126254-31126269 chr6:31126257-31126272 chr6:31126257-31126271 chr6:31126257-31126272
38	POLR2A	chr6:31126199-31126844	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr6:31125790-31126597	GM19193	blood:	n/a	n/a
40	FOS	chr6:31125998-31126278	MCF10A-Er-Src	breast:	n/a	n/a
41	ZNF263	chr6:31125975-31126926	HEK293-T-REx	kidney:	n/a	chr6:31126064-31126073 chr6:31126065-31126086 chr6:31126854-31126863
42	POLR2A	chr6:31125665-31126576	SK-N-SH	brain:	n/a	n/a
43	HMGN3	chr6:31125847-31126599	K562	blood:	n/a	n/a
44	MAFF	chr6:31126060-31126422	HepG2	liver:	n/a	n/a
45	POLR2A	chr6:31125664-31126621	PANC-1	pancreas:	n/a	n/a
46	TCF7L2	chr6:31126145-31126336	PANC-1	pancreas:	n/a	n/a
47	KAP1	chr6:31126153-31126647	HEK293	kidney:	n/a	chr6:31126591-31126599
48	ZNF143	chr6:31125874-31126426	GM12878	blood:	n/a	n/a
49	SIN3AK20	chr6:31126191-31126620	A549	lung:	n/a	n/a
50	MAZ	chr6:31125452-31126914	IMR90	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31125954..31128399-chr6:31147370..31149956,2	MCF-7	breast:
2	chr6:31124835..31127745-chr6:31135310..31138711,4	MCF-7	breast:
3	chr6:30584033..30586510-chr6:31124123..31126779,2	K562	blood:
4	chr6:31119377..31122828-chr6:31124699..31127188,7	K562	blood:
5	chr20:30192973..30193725-chr6:31125491..31126289,2	HCT-116	colon:
6	chr2:113032954..113033816-chr6:31125777..31126493,2	HCT-116	colon:
7	chr6:31103871..31105834-chr6:31123155..31127372,3	MCF-7	breast:
8	chr6:31103022..31109591-chr6:31125707..31129394,9	MCF-7	breast:
9	chr6:31120552..31122855-chr6:31123459..31126942,6	MCF-7	breast:

Variant related genes	Relation type
CCHCR1	TF binding region
TCF19	TF binding region
ENSG00000222894	Chromatin interaction
ENSG00000188177	Chromatin interaction
ENSG00000204568	Chromatin interaction
ENSG00000204540	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000204531	Chromatin interaction
ENSG00000125968	Chromatin interaction
ENSG00000238211	Chromatin interaction
ENSG00000204538	Chromatin interaction
ENSG00000204536	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1044870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1063646	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11758495	0.86[ASN][1000 genomes]
rs12364	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs130077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17190589	0.83[ASN][1000 genomes]
rs2233945	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2233946	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2233947	0.93[ASN][1000 genomes]
rs28742577	0.86[ASN][1000 genomes]
rs35157432	0.83[ASN][1000 genomes]
rs62398706	0.86[ASN][1000 genomes]
rs62400570	0.80[ASN][1000 genomes]
rs6903261	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6909939	0.86[AFR][1000 genomes]
rs6910473	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6913074	0.93[ASN][1000 genomes]
rs7757012	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7771067	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9263708	0.83[ASN][1000 genomes]
rs9263733	0.93[ASN][1000 genomes]
rs9263738	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9263739	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9263741	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9263745	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263749	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9263750	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9263751	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9263756	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9263766	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263768	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263769	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9263774	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263775	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263776	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263777	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263778	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263781	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263785	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263792	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263794	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9263796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9263800	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263802	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263809	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263810	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263811	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263816	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9263817	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263818	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9263822	0.86[ASN][1000 genomes]
rs9263825	0.93[ASN][1000 genomes]
rs9263827	0.86[ASN][1000 genomes]
rs9263832	0.86[ASN][1000 genomes]
rs9263833	0.93[ASN][1000 genomes]
rs9263838	0.93[ASN][1000 genomes]
rs9263843	0.86[ASN][1000 genomes]
rs9263855	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
5	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
6	nsv1029442	chr6:31006647-31449207	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
7	nsv427750	chr6:31028290-31234581	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv428140	chr6:31028290-31462106	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	89 gene(s)	inside rSNPs	diseases
9	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
10	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
11	nsv525933	chr6:31081205-31142245	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
12	nsv884137	chr6:31082361-31129310	Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
13	nsv1019637	chr6:31104401-31354706	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
14	nsv1029569	chr6:31104401-31412740	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
15	nsv538174	chr6:31104401-31412740	Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
16	nsv524061	chr6:31107087-31133943	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
17	nsv884138	chr6:31114573-31129707	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31124800-31126800	Active TSS	NHLF	lung
2	chr6:31125000-31127000	Active TSS	Muscle Satellite Cultured Cells	--
3	chr6:31125000-31127400	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr6:31125000-31127800	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr6:31125200-31126400	Active TSS	Primary hematopoietic stem cells	blood
6	chr6:31125200-31126800	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr6:31125200-31127400	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr6:31125200-31127800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr6:31125400-31126400	Active TSS	Right Ventricle	heart
10	chr6:31125400-31126600	Active TSS	Primary T helper cells PMA-I stimulated	--
11	chr6:31125400-31126600	Active TSS	Brain Angular Gyrus	brain
12	chr6:31125400-31126600	Active TSS	Brain Anterior Caudate	brain
13	chr6:31125400-31126600	Active TSS	Brain Cingulate Gyrus	brain
14	chr6:31125400-31126600	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr6:31125400-31126600	Active TSS	Duodenum Mucosa	Duodenum
16	chr6:31125400-31126600	Active TSS	Fetal Brain Male	brain
17	chr6:31125400-31126600	Active TSS	Fetal Brain Female	brain
18	chr6:31125400-31126600	Active TSS	Fetal Heart	heart
19	chr6:31125400-31126600	Active TSS	Fetal Intestine Large	intestine
20	chr6:31125400-31126600	Active TSS	Fetal Intestine Small	intestine
21	chr6:31125400-31126600	Active TSS	Fetal Stomach	stomach
22	chr6:31125400-31126600	Active TSS	Stomach Mucosa	stomach
23	chr6:31125400-31126600	Active TSS	HepG2	liver
24	chr6:31125400-31126600	Active TSS	HSMM	muscle
25	chr6:31125400-31126800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:31125400-31126800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:31125400-31126800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr6:31125400-31126800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:31125400-31126800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:31125400-31126800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:31125400-31126800	Active TSS	Brain Hippocampus Middle	brain
32	chr6:31125400-31126800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr6:31125400-31126800	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr6:31125400-31126800	Active TSS	Fetal Lung	lung
35	chr6:31125400-31126800	Active TSS	Left Ventricle	heart
36	chr6:31125400-31126800	Active TSS	Ovary	ovary
37	chr6:31125400-31126800	Active TSS	Psoas Muscle	Psoas
38	chr6:31125400-31126800	Active TSS	Rectal Smooth Muscle	rectum
39	chr6:31125400-31126800	Active TSS	K562	blood
40	chr6:31125400-31126800	Active TSS	Osteobl	bone
41	chr6:31125400-31127000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:31125400-31127000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:31125400-31127000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:31125400-31127000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:31125400-31127000	Active TSS	Esophagus	oesophagus
46	chr6:31125400-31127000	Active TSS	A549	lung
47	chr6:31125400-31127000	Active TSS	HMEC	breast
48	chr6:31125400-31127000	Active TSS	HSMMtube	muscle
49	chr6:31125400-31127200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:31125400-31127200	Active TSS	Colon Smooth Muscle	Colon

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