Variant report

Variant	esv3370662
Chromosome Location	chr10:976702-979450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:680)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:977654-977803	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:977720-977747	K562	blood:	n/a	n/a
3	ATF1	chr10:977597-977929	K562	blood:	n/a	n/a
4	ATF2	chr10:977473-977853	GM12878	blood:	n/a	n/a
5	BACH1	chr10:976720-976818	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr10:976320-976797	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:975896-976809	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:977609-978009	HepG2	liver:	n/a	n/a
9	BHLHE40	chr10:977554-978115	K562	blood:	n/a	n/a
10	BHLHE40	chr10:977582-978159	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:976476-976810	K562	blood:	n/a	n/a
12	BRCA1	chr10:977564-977827	GM12878	blood:	n/a	n/a
13	BRCA1	chr10:977555-977858	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr10:977585-977787	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr10:976675-978128	K562	blood:	n/a	n/a
16	CEBPB	chr10:977489-977746	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:977550-977764	K562	blood:	n/a	n/a
18	CEBPB	chr10:977555-977810	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:977648-977792	A549	lung:	n/a	n/a
20	CHD1	chr10:975406-978308	IMR90	lung:	n/a	chr10:977804-977814 chr10:977690-977700
21	CHD1	chr10:975847-976842	GM12878	blood:	n/a	n/a
22	CHD1	chr10:976545-976804	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr10:977519-977905	HepG2	liver:	n/a	chr10:977804-977814 chr10:977690-977700
24	CHD2	chr10:977450-977923	K562	blood:	n/a	chr10:977804-977814 chr10:977690-977700
25	CHD2	chr10:977544-977899	H1-hESC	embryonic stem cell:	n/a	chr10:977804-977814 chr10:977690-977700
26	CHD2	chr10:976708-976964	HepG2	liver:	n/a	n/a
27	CHD2	chr10:977494-977954	GM12878	blood:	n/a	chr10:977804-977814 chr10:977690-977700
28	CHD2	chr10:977439-978125	Hela-S3	cervix:	n/a	chr10:977804-977814 chr10:977690-977700
29	CHD2	chr10:976657-976885	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr10:976657-976873	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr10:977494-978233	HepG2	liver:	n/a	n/a
32	CREB1	chr10:977542-977906	A549	lung:	n/a	n/a
33	CREB1	chr10:977505-978018	ECC-1	luminal epithelium:	n/a	n/a
34	CREB1	chr10:977403-978344	HepG2	liver:	n/a	n/a
35	CREB1	chr10:977174-978193	A549	lung:	n/a	n/a
36	CREB1	chr10:977416-978202	GM12878	blood:	n/a	n/a
37	CREB1	chr10:977535-978186	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr10:977528-978077	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr10:976607-976960	A549	lung:	n/a	n/a
40	CREB1	chr10:977487-978028	K562	blood:	n/a	n/a
41	CTCF	chr10:976820-976970	GM12869	blood:	n/a	chr10:976876-976889
42	CTCF	chr10:976740-976890	SK-N-SH_RA	brain:	n/a	chr10:976876-976889
43	CTCF	chr10:976813-976916	ProgFib	skin:	n/a	chr10:976876-976889
44	CTCF	chr10:977900-978050	AG04449	skin:	n/a	n/a
45	CTCF	chr10:976762-976944	GM19240	blood:	n/a	chr10:976876-976889
46	CTCF	chr10:977960-978110	HMEC	breast:	n/a	n/a
47	CTCF	chr10:976800-976950	GM12868	blood:	n/a	chr10:976876-976889
48	CTCF	chr10:976841-976946	H1-hESC	embryonic stem cell:	n/a	chr10:976876-976889
49	CTCF	chr10:976808-976952	MCF-7	breast:	n/a	chr10:976876-976889
50	CTCF	chr10:976808-976927	A549	lung:	n/a	chr10:976876-976889

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:976940-976990	K562	blood:	n/a
2	chr10:978077-978127	NH-A	brain:	n/a
3	chr10:978077-978127	PANC-1	pancreas:	n/a
4	chr10:978019-978069	MCF-7	breast:	n/a
5	chr10:977622-977672	HepG2	liver:	n/a
6	chr10:978019-978069	SK-N-MC	brain:	n/a
7	chr10:977622-977672	H1-hESC	embryonic stem cell:	embryo
8	chr10:978019-978069	HCPEpiC	choroid plexus:	n/a
9	chr10:978019-978069	K562	blood:	n/a
10	chr10:977622-977672	CMK	blood:	n/a
11	chr10:978077-978127	GM06990	blood:	n/a
12	chr10:978019-978069	Hela-S3	cervix:	n/a
13	chr10:978077-978127	IMR90	lung:	fetal
14	chr10:977622-977672	HEEpiC	esophagus:	n/a
15	chr10:976940-976990	SK-N-MC	brain:	n/a
16	chr10:978019-978069	PrEC	prostate:	n/a
17	chr10:976940-976990	ECC-1	luminal epithelium:	n/a
18	chr10:978019-978069	SAEC	small airway:	n/a
19	chr10:978019-978069	BE2_C	brain:	n/a
20	chr10:978019-978069	HNPCEpiC	eye:	n/a
21	chr10:977622-977672	Caco-2	colon:	n/a
22	chr10:976940-976990	GM12892	blood:	n/a
23	chr10:977622-977672	NT2-D1	testis:	n/a
24	chr10:978019-978069	HRCEpiC	kidney:	n/a
25	chr10:978077-978127	HUVEC	blood vessel:	n/a
26	chr10:978019-978069	CMK	blood:	n/a
27	chr10:978077-978127	NT2-D1	testis:	n/a
28	chr10:977622-977672	GM19239	blood:	n/a
29	chr10:978077-978127	U87	brain:	n/a
30	chr10:977622-977672	HCF	heart:	n/a
31	chr10:977622-977672	HCPEpiC	choroid plexus:	n/a
32	chr10:978019-978069	RPTEC	kidney:	n/a
33	chr10:978077-978127	Hepatocyte	liver:	n/a
34	chr10:978077-978127	AG04449	skin:	fetal
35	chr10:976940-976990	GM12891	blood:	n/a
36	chr10:978019-978069	H1-hESC	embryonic stem cell:	embryo
37	chr10:978019-978069	ProgFib	skin:	n/a
38	chr10:978077-978127	MCF-7	breast:	n/a
39	chr10:976940-976990	GM06990	blood:	n/a
40	chr10:978077-978127	NHDF-neo	bronchial:	n/a
41	chr10:978077-978127	HRCEpiC	kidney:	n/a
42	chr10:978019-978069	GM19239	blood:	n/a
43	chr10:976940-976990	AG10803	skin:	n/a
44	chr10:978077-978127	GM12891	blood:	n/a
45	chr10:978019-978069	GM06990	blood:	n/a
46	chr10:976940-976990	HCM	heart:	n/a
47	chr10:977622-977672	HUVEC	blood vessel:	n/a
48	chr10:978077-978127	ECC-1	luminal epithelium:	n/a
49	chr10:978077-978127	MCF10A-Er-Src	breast:	n/a
50	chr10:977622-977672	SK-N-SH_RA	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
2	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
3	chr10:975582..978698-chr10:1119494..1122267,3	MCF-7	breast:
4	chr10:974636..980819-chr10:1029938..1037009,15	MCF-7	breast:
5	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
6	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
7	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
8	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
9	chr10:974758..976966-chr10:1110782..1112393,2	MCF-7	breast:
10	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
11	chr10:976553..979064-chr17:56707717..56709888,2	MCF-7	breast:
12	chr10:976566..978917-chr20:33411823..33413821,2	MCF-7	breast:
13	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
14	chr10:975309..980832-chr10:1031626..1035973,12	K562	blood:
15	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
16	chr10:977686..978278-chr3:23958133..23959063,2	HCT-116	colon:
17	chr10:979434..982350-chr10:995576..997645,2	MCF-7	breast:
18	chr10:974758..977274-chr10:1018618..1021450,2	K562	blood:
19	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP4-3	chr10:978420-978683	NONHSAT010879
2	lnc-GTPBP4-3	chr10:978966-979055	ENSG00000229869.1
3	lnc-GTPBP4-3	chr10:978127-978179	NONHSAT010879

No data

Variant related genes	Relation type
ENSG00000229869	TF binding region
LARP4B	TF binding region
ENSG00000229869	CpG island
LARP4B	CpG island
ENSG00000047056	chromatin interactions
ENSG00000198646	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000205740	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 76 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:76 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562080657	chr10:976707-976708	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs572142454	chr10:976813-976814	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs569931707	chr10:976826-976827	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs535655879	chr10:976897-976898	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs375133750	chr10:976924-976925	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs565808559	chr10:977016-977017	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs534403452	chr10:977066-977067	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs557761886	chr10:977086-977087	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs577585865	chr10:977114-977115	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs111734794	chr10:977123-977124	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs557238299	chr10:977129-977130	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs573951281	chr10:977144-977145	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs539210260	chr10:977187-977188	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs372505958	chr10:977224-977225	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs542862487	chr10:977280-977281	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs545507889	chr10:977312-977313	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs7082265	chr10:977341-977342	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs7095754	chr10:977437-977438	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs201543910	chr10:977552-977553	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs559512960	chr10:977600-977601	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs372473714	chr10:977644-977645	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs558434664	chr10:977829-977830	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs573323851	chr10:977885-977886	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs375761508	chr10:977911-977912	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs545151590	chr10:977976-977977	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs565352580	chr10:978005-978006	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs530826461	chr10:978026-978027	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs550953923	chr10:978044-978045	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs563619920	chr10:978168-978169	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
30	rs368588471	chr10:978202-978203	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs529192603	chr10:978236-978237	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs549232087	chr10:978238-978239	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs540905718	chr10:978261-978262	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs181737840	chr10:978266-978267	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs184911478	chr10:978269-978270	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs565714551	chr10:978281-978282	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs534786139	chr10:978287-978288	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs112000211	chr10:978315-978316	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs113757740	chr10:978319-978320	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs551202129	chr10:978321-978322	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs571277257	chr10:978322-978323	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs111079693	chr10:978325-978326	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs186126648	chr10:978337-978338	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs113211985	chr10:978364-978365	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs189811803	chr10:978374-978375	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs71494940	chr10:978466-978467	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
47	rs113408700	chr10:978509-978510	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
48	rs536650013	chr10:978610-978611	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
49	rs556538387	chr10:978662-978663	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
50	rs574038777	chr10:978672-978673	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:974600-976800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:975200-979200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:975400-976800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:975400-976800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr10:975600-978400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr10:975600-978400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr10:975600-978400	Active TSS	GM12878-XiMat	blood
8	chr10:975600-978800	Active TSS	Psoas Muscle	Psoas
9	chr10:975600-979000	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr10:975800-976800	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr10:975800-977200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr10:975800-978200	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr10:975800-978200	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr10:975800-978200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:975800-978400	Active TSS	H9 Cell Line	embryonic stem cell
16	chr10:975800-978400	Active TSS	Fetal Intestine Large	intestine
17	chr10:975800-978400	Active TSS	NHLF	lung
18	chr10:976000-976800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
19	chr10:976000-976800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
20	chr10:976000-976800	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr10:976000-976800	Flanking Active TSS	Brain Germinal Matrix	brain
22	chr10:976000-976800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
23	chr10:976000-976800	Flanking Active TSS	Fetal Brain Male	brain
24	chr10:976000-976800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr10:976000-977200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr10:976000-978200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr10:976000-978200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr10:976000-978200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:976000-978200	Active TSS	HSMMtube	muscle
30	chr10:976000-978400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr10:976000-978400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr10:976000-978400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr10:976000-978400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr10:976000-978400	Active TSS	Esophagus	oesophagus
35	chr10:976000-978400	Active TSS	Fetal Intestine Small	intestine
36	chr10:976000-978400	Active TSS	Monocytes-CD14+_RO01746	blood
37	chr10:976000-978600	Active TSS	Ovary	ovary
38	chr10:976200-976800	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr10:976200-976800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr10:976200-976800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr10:976200-976800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr10:976200-976800	Active TSS	Fetal Kidney	kidney
43	chr10:976200-977000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr10:976200-977200	Active TSS	Stomach Mucosa	stomach
45	chr10:976200-978200	Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr10:976200-978200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr10:976200-978200	Active TSS	Rectal Mucosa Donor 29	rectum
48	chr10:976200-978200	Active TSS	Sigmoid Colon	Sigmoid Colon
49	chr10:976200-978200	Active TSS	Small Intestine	intestine
50	chr10:976200-978200	Active TSS	NHDF-Ad	bronchial

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