Variant report

Variant	nsv891151
Chromosome Location	chr8:87690019-87776019
allele	n/a
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	ARID3A	chr8:87715605-87715931	HepG2	liver:	n/a	n/a
2	ATF2	chr8:87718380-87718825	GM12878	blood:	n/a	n/a
3	ATF3	chr8:87757059-87757437	HCT-116	colon:	n/a	n/a
4	BACH1	chr8:87727067-87727263	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:87719573-87719917	GM12878	blood:	n/a	n/a
6	BATF	chr8:87718793-87719078	GM12878	blood:	n/a	n/a
7	BATF	chr8:87719574-87719931	GM12878	blood:	n/a	n/a
8	BCLAF1	chr8:87715534-87715980	GM12878	blood:	n/a	chr8:87715668-87715677
9	BHLHE40	chr8:87719747-87719791	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:87718453-87719024	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:87727116-87727254	GM12878	blood:	n/a	n/a
12	BRCA1	chr8:87742754-87742780	GM12878	blood:	n/a	n/a
13	CEBPB	chr8:87699742-87699900	K562	blood:	n/a	chr8:87699846-87699857
14	CEBPB	chr8:87699662-87700017	H1-hESC	embryonic stem cell:	n/a	chr8:87699846-87699857
15	CEBPB	chr8:87773226-87773407	HepG2	liver:	n/a	chr8:87773328-87773339
16	CEBPB	chr8:87699667-87700036	A549	lung:	n/a	chr8:87699846-87699857
17	CEBPB	chr8:87699664-87700345	Hela-S3	cervix:	n/a	chr8:87699846-87699857
18	CEBPB	chr8:87749774-87749955	A549	lung:	n/a	n/a
19	CEBPB	chr8:87699656-87700041	K562	blood:	n/a	chr8:87699846-87699857
20	CEBPB	chr8:87699633-87700036	ECC-1	luminal epithelium:	n/a	chr8:87699846-87699857
21	CEBPB	chr8:87699682-87699968	ECC-1	luminal epithelium:	n/a	chr8:87699846-87699857
22	CEBPB	chr8:87699521-87700079	MCF-7	breast:	n/a	chr8:87699846-87699857
23	CEBPB	chr8:87699611-87700083	A549	lung:	n/a	chr8:87699846-87699857
24	CEBPB	chr8:87699652-87700042	IMR90	lung:	n/a	chr8:87699846-87699857
25	CEBPB	chr8:87699668-87700031	HepG2	liver:	n/a	chr8:87699846-87699857
26	CEBPB	chr8:87722173-87722348	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:87699632-87699959	A549	lung:	n/a	chr8:87699846-87699857
28	CEBPB	chr8:87699637-87700086	MCF-7	breast:	n/a	chr8:87699846-87699857
29	CEBPB	chr8:87742357-87742598	A549	lung:	n/a	n/a
30	CHD2	chr8:87727020-87727220	GM12878	blood:	n/a	n/a
31	CTCF	chr8:87715740-87715890	NHLF	lung:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
32	CTCF	chr8:87715720-87715870	NB4	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
33	CTCF	chr8:87715700-87715850	HA-sp	spinal cord:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
34	CTCF	chr8:87715636-87715841	A549	lung:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
35	CTCF	chr8:87715660-87715810	MCF-7	breast:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
36	CTCF	chr8:87715700-87715850	GM12874	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
37	CTCF	chr8:87715720-87715870	GM12869	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
38	CTCF	chr8:87715700-87715850	GM12875	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
39	CTCF	chr8:87715637-87715905	ProgFib	skin:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
40	CTCF	chr8:87710893-87710998	Lung_OC	lung:	n/a	n/a
41	CTCF	chr8:87715643-87715880	Pancreas_OC	pancreas:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
42	CTCF	chr8:87715700-87715850	GM12878	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
43	CTCF	chr8:87715680-87715830	GM12875	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
44	CTCF	chr8:87715680-87715830	K562	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
45	CTCF	chr8:87715720-87715870	GM06990	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
46	CTCF	chr8:87715447-87716043	MCF-7	breast:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
47	CTCF	chr8:87715641-87715913	SK-N-SH_RA	brain:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
48	CTCF	chr8:87715620-87715770	GM06990	blood:	n/a	n/a
49	CTCF	chr8:87715740-87715890	HVMF	connective:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772
50	CTCF	chr8:87715581-87715932	K562	blood:	n/a	chr8:87715759-87715777 chr8:87715761-87715782 chr8:87715764-87715772

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:87755844-87755894	PFSK-1	brain:	n/a
2	chr8:87756528-87756578	HMEC	breast:	n/a
3	chr8:87755844-87755894	MCF-7	breast:	n/a
4	chr8:87721838-87721888	HL-60	blood:	n/a
5	chr8:87756528-87756578	HNPCEpiC	eye:	n/a
6	chr8:87757285-87757335	BJ	skin:	n/a
7	chr8:87755844-87755894	HRCEpiC	kidney:	n/a
8	chr8:87757285-87757335	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:87756528-87756578	HRCEpiC	kidney:	n/a
10	chr8:87721838-87721888	LNCaP	prostate:	n/a
11	chr8:87757285-87757335	ProgFib	skin:	n/a
12	chr8:87756528-87756578	BJ	skin:	n/a
13	chr8:87755844-87755894	HEEpiC	esophagus:	n/a
14	chr8:87757285-87757335	SAEC	small airway:	n/a
15	chr8:87721838-87721888	HEK293	kidney:	embryo
16	chr8:87757285-87757335	Hela-S3	cervix:	n/a
17	chr8:87755844-87755894	HRPEpiC	eye:	n/a
18	chr8:87756528-87756578	Caco-2	colon:	n/a
19	chr8:87756528-87756578	GM12878	blood:	n/a
20	chr8:87757285-87757335	AoSMC	blood vessel:	n/a
21	chr8:87755844-87755894	K562	blood:	n/a
22	chr8:87721838-87721888	CMK	blood:	n/a
23	chr8:87757285-87757335	GM06990	blood:	n/a
24	chr8:87721838-87721888	HIPEpiC	eye:	n/a
25	chr8:87755844-87755894	U87	brain:	n/a
26	chr8:87755844-87755894	HCPEpiC	choroid plexus:	n/a
27	chr8:87756528-87756578	MCF-7	breast:	n/a
28	chr8:87755844-87755894	BJ	skin:	n/a
29	chr8:87721838-87721888	ECC-1	luminal epithelium:	n/a
30	chr8:87755844-87755894	NT2-D1	testis:	n/a
31	chr8:87757285-87757335	IMR90	lung:	fetal
32	chr8:87757285-87757335	Caco-2	colon:	n/a
33	chr8:87756528-87756578	HUVEC	blood vessel:	n/a
34	chr8:87755844-87755894	RPTEC	kidney:	n/a
35	chr8:87755844-87755894	CMK	blood:	n/a
36	chr8:87757285-87757335	NH-A	brain:	n/a
37	chr8:87756528-87756578	GM12891	blood:	n/a
38	chr8:87756528-87756578	SK-N-SH	brain:	n/a
39	chr8:87756528-87756578	T-47D	breast:	n/a
40	chr8:87757285-87757335	H1-hESC	embryonic stem cell:	embryo
41	chr8:87755844-87755894	GM19239	blood:	n/a
42	chr8:87755844-87755894	ovcar-3	ovarian:	n/a
43	chr8:87756528-87756578	AG09309	skin:	n/a
44	chr8:87756528-87756578	HCF	heart:	n/a
45	chr8:87721838-87721888	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:87721838-87721888	K562	blood:	n/a
47	chr8:87755844-87755894	NB4	blood:	n/a
48	chr8:87721838-87721888	HCT-116	colon:	n/a
49	chr8:87755844-87755894	MCF10A-Er-Src	breast:	n/a
50	chr8:87721838-87721888	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr8:87715321..87715869-chr8:87882947..87883942,2	MCF-7	breast:
2	chr8:87715109..87716653-chr8:87797088..87798149,7	MCF-7	breast:
3	chr8:87712105..87713974-chr8:87796299..87798586,2	MCF-7	breast:
4	chr1:205628182..205628700-chr8:87715530..87716219,2	MCF-7	breast:
5	chr8:87713968..87715831-chr8:90615267..90617535,2	K562	blood:
6	chr8:87630993..87631693-chr8:87715283..87716117,3	MCF-7	breast:
7	chr8:87570422..87571030-chr8:87715384..87716149,2	MCF-7	breast:
8	chr8:87632935..87634683-chr8:87691682..87694480,2	MCF-7	breast:
9	chr8:87682795..87685163-chr8:87691577..87693965,2	MCF-7	breast:
10	chr8:87764977..87767353-chr8:87767887..87770329,2	MCF-7	breast:
11	chr8:87715130..87716346-chr8:87797049..87798098,25	MCF-7	breast:
12	chr8:87715350..87716057-chr8:87779206..87780134,2	MCF-7	breast:
13	chr8:87715699..87716286-chr8:87798755..87799414,2	MCF-7	breast:
14	chr8:87715306..87716350-chr8:87803816..87804906,11	MCF-7	breast:
15	chr8:87764977..87767353-chr8:87767887..87770329,2	MCF-7	breast:
16	chr8:87715318..87716419-chr8:87803806..87804632,5	MCF-7	breast:
17	chr20:52195243..52195928-chr8:87697901..87698886,2	MCF-7	breast:
18	chr8:87717437..87718015-chr8:87797121..87797669,2	MCF-7	breast:
19	chr8:87715292..87715843-chr8:90701514..90702072,2	K562	blood:
20	chr8:87715050..87716703-chr8:87803465..87805909,2	MCF-7	breast:
21	chr8:87753635..87756349-chr8:87759973..87762322,2	MCF-7	breast:
22	chr8:87715640..87716182-chr8:87795719..87796695,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM82B-2	chr8:87716177-87716630	NONHSAT127568
2	lnc-CNBD1-2	chr8:87773064-87773188	ENSG00000254115.1
3	lnc-FAM82B-2	chr8:87755727-87755837	NONHSAT127568
4	lnc-FAM82B-2	chr8:87751883-87751964	NONHSAT127568
5	lnc-CNBD1-2	chr8:87719775-87720222	ENSG00000254115.1
6	lnc-FAM82B-2	chr8:87738759-87738885	NONHSAT127568

Variant related genes	Relation type
ENSG00000253778	TF binding region
CNGB3	TF binding region
ENSG00000254115	TF binding region
ENSG00000253778	CpG island
CNGB3	CpG island
ENSG00000254115	CpG island
ENSG00000170289	chromatin interactions

Extended variants
information (count: 2198 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140195806	chr8:87695005-87695006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79642808	chr8:87695026-87695027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558830904	chr8:87695067-87695068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377650690	chr8:87695087-87695088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554664474	chr8:87695169-87695170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190342275	chr8:87695187-87695188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182680193	chr8:87695201-87695202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553764179	chr8:87695204-87695205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143797234	chr8:87695304-87695305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73273357	chr8:87695327-87695328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146377468	chr8:87695328-87695329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187007959	chr8:87695389-87695390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190901256	chr8:87695410-87695411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569477110	chr8:87695411-87695412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182781043	chr8:87695437-87695438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532511694	chr8:87695449-87695450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77969655	chr8:87695465-87695466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559722911	chr8:87695475-87695476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536830024	chr8:87695492-87695493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139364764	chr8:87695522-87695523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569871299	chr8:87695530-87695531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558765430	chr8:87695551-87695552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370492166	chr8:87695588-87695589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576000341	chr8:87697428-87697429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4960988	chr8:87697496-87697497	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573321224	chr8:87697509-87697510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540802657	chr8:87697527-87697528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562169416	chr8:87697535-87697536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529586546	chr8:87697563-87697564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544959894	chr8:87697576-87697577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12676456	chr8:87697646-87697647	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7832818	chr8:87697647-87697648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs111813106	chr8:87697683-87697684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140842443	chr8:87697819-87697820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184531871	chr8:87697822-87697823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373177741	chr8:87697828-87697829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568204027	chr8:87697829-87697830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188991627	chr8:87697864-87697865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182432650	chr8:87697895-87697896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77854843	chr8:87697910-87697911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539462732	chr8:87697923-87697924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs13268968	chr8:87697961-87697962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs573262859	chr8:87697969-87697970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186223252	chr8:87697972-87697973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527739465	chr8:87712000-87712001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549478877	chr8:87712003-87712004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562738374	chr8:87712030-87712031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533723262	chr8:87712085-87712086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187540800	chr8:87712092-87712093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62525677	chr8:87712117-87712118	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Prostate cancer	20978177	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87695000-87695600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:87697400-87698000	Enhancers	Colon Smooth Muscle	Colon
3	chr8:87712000-87712200	Enhancers	Fetal Brain Male	brain
4	chr8:87712200-87713200	Weak transcription	Fetal Brain Male	brain
5	chr8:87713200-87713800	Enhancers	Fetal Brain Male	brain
6	chr8:87713800-87715600	Weak transcription	Fetal Brain Male	brain
7	chr8:87715400-87715600	Enhancers	Brain Anterior Caudate	brain
8	chr8:87715600-87716000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:87715600-87716000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:87715600-87716000	Flanking Active TSS	Brain Anterior Caudate	brain
11	chr8:87715600-87716000	Enhancers	Brain Hippocampus Middle	brain
12	chr8:87715600-87716000	Enhancers	Fetal Brain Male	brain
13	chr8:87715600-87717000	Enhancers	Brain Germinal Matrix	brain
14	chr8:87715800-87716000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr8:87715800-87716000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:87715800-87716000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr8:87715800-87716000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:87715800-87716000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr8:87715800-87716000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr8:87715800-87716000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr8:87715800-87716000	Enhancers	Liver	Liver
22	chr8:87715800-87716000	Enhancers	Brain Angular Gyrus	brain
23	chr8:87715800-87716000	Enhancers	Brain Cingulate Gyrus	brain
24	chr8:87715800-87716000	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr8:87715800-87716000	Enhancers	Fetal Lung	lung
26	chr8:87715800-87716000	Enhancers	Fetal Stomach	stomach
27	chr8:87715800-87716000	Enhancers	Psoas Muscle	Psoas
28	chr8:87715800-87716000	Enhancers	Right Atrium	heart
29	chr8:87715800-87716000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr8:87715800-87716000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr8:87715800-87716000	Enhancers	HUVEC	blood vessel
32	chr8:87715800-87716000	Enhancers	Osteobl	bone
33	chr8:87715800-87716600	Enhancers	Fetal Kidney	kidney
34	chr8:87715800-87717200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr8:87715800-87719200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:87716000-87717200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:87716000-87717200	Weak transcription	Fetal Stomach	stomach
38	chr8:87716000-87717800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:87716000-87718000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:87716000-87718400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:87716000-87718600	Weak transcription	Osteobl	bone
42	chr8:87716000-87721400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr8:87716000-87721600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:87716200-87716400	Enhancers	Fetal Brain Female	brain
45	chr8:87716200-87718600	Weak transcription	HUVEC	blood vessel
46	chr8:87716400-87718400	Weak transcription	Fetal Brain Female	brain
47	chr8:87716800-87717400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr8:87717200-87717400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:87717200-87718000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr8:87717200-87718000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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