Variant report

Variant	nsv1026680
Chromosome Location	chr8:111131741-111413284
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	chr8:111173265-111173927	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:111370803-111370846	K562	blood:	n/a	n/a
3	BACH1	chr8:111361264-111361282	K562	blood:	n/a	n/a
4	BATF	chr8:111380529-111380748	GM12878	blood:	n/a	n/a
5	BATF	chr8:111173464-111173734	GM12878	blood:	n/a	chr8:111173573-111173584
6	BATF	chr8:111173429-111173788	GM12878	blood:	n/a	chr8:111173573-111173584
7	BATF	chr8:111380515-111380775	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:111221834-111221837	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:111133833-111134173	A549	lung:	n/a	chr8:111133993-111134004
10	CEBPB	chr8:111140081-111140301	HepG2	liver:	n/a	chr8:111140236-111140247 chr8:111140220-111140231
11	CEBPB	chr8:111202881-111203080	HepG2	liver:	n/a	chr8:111202975-111202986 chr8:111202974-111202987 chr8:111202974-111202987
12	CEBPB	chr8:111173453-111173826	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:111133794-111134166	HepG2	liver:	n/a	chr8:111133993-111134004
14	CEBPB	chr8:111326176-111326371	K562	blood:	n/a	chr8:111326272-111326283
15	CEBPB	chr8:111326111-111326430	HepG2	liver:	n/a	chr8:111326272-111326283
16	CEBPB	chr8:111224207-111224474	HepG2	liver:	n/a	chr8:111224294-111224305
17	CEBPB	chr8:111183605-111183719	H1-hESC	embryonic stem cell:	n/a	chr8:111183671-111183682
18	CEBPB	chr8:111133852-111134167	IMR90	lung:	n/a	chr8:111133993-111134004
19	CEBPB	chr8:111407025-111407692	A549	lung:	n/a	chr8:111407634-111407645 chr8:111407125-111407136
20	CEBPB	chr8:111183596-111183769	HepG2	liver:	n/a	chr8:111183671-111183682
21	CEBPB	chr8:111407057-111407265	HepG2	liver:	n/a	chr8:111407125-111407136
22	CEBPB	chr8:111311551-111311683	H1-hESC	embryonic stem cell:	n/a	chr8:111311652-111311663
23	CEBPB	chr8:111346863-111346939	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:111133898-111134083	HepG2	liver:	n/a	chr8:111133993-111134004
25	CEBPB	chr8:111407619-111407631	K562	blood:	n/a	n/a
26	CEBPB	chr8:111209359-111209680	HepG2	liver:	n/a	chr8:111209521-111209532
27	CEBPB	chr8:111133935-111134082	K562	blood:	n/a	chr8:111133993-111134004
28	CEBPB	chr8:111271067-111271189	HepG2	liver:	n/a	chr8:111271123-111271134
29	CEBPB	chr8:111154536-111154851	IMR90	lung:	n/a	chr8:111154554-111154567 chr8:111154708-111154719
30	CEBPB	chr8:111407564-111407694	HepG2	liver:	n/a	chr8:111407634-111407645
31	CEBPB	chr8:111180761-111180946	A549	lung:	n/a	n/a
32	CEBPB	chr8:111149718-111149935	HepG2	liver:	n/a	chr8:111149779-111149790
33	CEBPB	chr8:111209394-111209675	A549	lung:	n/a	chr8:111209521-111209532
34	CEBPB	chr8:111189639-111189974	MCF-7	breast:	n/a	chr8:111189781-111189792 chr8:111189779-111189792 chr8:111189779-111189790
35	CEBPB	chr8:111204483-111204631	HepG2	liver:	n/a	chr8:111204518-111204529
36	CEBPB	chr8:111392636-111392756	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:111133913-111134088	H1-hESC	embryonic stem cell:	n/a	chr8:111133993-111134004
38	CEBPB	chr8:111133808-111134191	HepG2	liver:	n/a	chr8:111133993-111134004
39	CEBPB	chr8:111140084-111140231	K562	blood:	n/a	chr8:111140220-111140231
40	CEBPB	chr8:111348693-111348897	A549	lung:	n/a	n/a
41	CEBPB	chr8:111326135-111326438	IMR90	lung:	n/a	chr8:111326272-111326283
42	CEBPB	chr8:111326108-111326428	A549	lung:	n/a	chr8:111326272-111326283
43	CEBPB	chr8:111133834-111134178	MCF-7	breast:	n/a	chr8:111133993-111134004
44	CEBPB	chr8:111189700-111189932	H1-hESC	embryonic stem cell:	n/a	chr8:111189781-111189792 chr8:111189779-111189792 chr8:111189779-111189790
45	CEBPB	chr8:111154566-111154822	HepG2	liver:	n/a	chr8:111154708-111154719
46	CEBPB	chr8:111189653-111189976	HepG2	liver:	n/a	chr8:111189781-111189792 chr8:111189779-111189792 chr8:111189779-111189790
47	CEBPB	chr8:111311571-111311766	HepG2	liver:	n/a	chr8:111311652-111311663
48	CEBPB	chr8:111311633-111311681	A549	lung:	n/a	chr8:111311652-111311663
49	CEBPB	chr8:111189681-111189971	IMR90	lung:	n/a	chr8:111189781-111189792 chr8:111189779-111189792 chr8:111189779-111189790
50	CEBPB	chr8:111209359-111209681	IMR90	lung:	n/a	chr8:111209521-111209532

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111214984-111215034	AG04449	skin:	fetal
2	chr8:111342449-111342499	SK-N-MC	brain:	n/a
3	chr8:111214984-111215034	Hepatocyte	liver:	n/a
4	chr8:111190216-111190266	MCF-7	breast:	n/a
5	chr8:111214984-111215034	SAEC	small airway:	n/a
6	chr8:111214984-111215034	MCF10A-Er-Src	breast:	n/a
7	chr8:111190216-111190266	HRPEpiC	eye:	n/a
8	chr8:111342449-111342499	SKMC	muscle:	n/a
9	chr8:111342449-111342499	PrEC	prostate:	n/a
10	chr8:111190216-111190266	Hepatocyte	liver:	n/a
11	chr8:111190216-111190266	U87	brain:	n/a
12	chr8:111214984-111215034	AG09319	gingival:	n/a
13	chr8:111342449-111342499	A549	lung:	n/a
14	chr8:111190216-111190266	PANC-1	pancreas:	n/a
15	chr8:111214984-111215034	HMEC	breast:	n/a
16	chr8:111190216-111190266	NHDF-neo	bronchial:	n/a
17	chr8:111342449-111342499	Hela-S3	cervix:	n/a
18	chr8:111190216-111190266	RPTEC	kidney:	n/a
19	chr8:111342449-111342499	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:111342449-111342499	NT2-D1	testis:	n/a
21	chr8:111190216-111190266	HPAEpiC	pulmonary alveolar:	n/a
22	chr8:111190216-111190266	Caco-2	colon:	n/a
23	chr8:111342449-111342499	GM06990	blood:	n/a
24	chr8:111214984-111215034	HAEpiC	amniotic membrane:	n/a
25	chr8:111214984-111215034	A549	lung:	n/a
26	chr8:111190216-111190266	SAEC	small airway:	n/a
27	chr8:111214984-111215034	T-47D	breast:	n/a
28	chr8:111190216-111190266	HIPEpiC	eye:	n/a
29	chr8:111214984-111215034	SKMC	muscle:	n/a
30	chr8:111190216-111190266	NT2-D1	testis:	n/a
31	chr8:111214984-111215034	NH-A	brain:	n/a
32	chr8:111214984-111215034	BJ	skin:	n/a
33	chr8:111214984-111215034	HCF	heart:	n/a
34	chr8:111190216-111190266	NH-A	brain:	n/a
35	chr8:111190216-111190266	AG09309	skin:	n/a
36	chr8:111342449-111342499	HNPCEpiC	eye:	n/a
37	chr8:111214984-111215034	GM06990	blood:	n/a
38	chr8:111214984-111215034	HNPCEpiC	eye:	n/a
39	chr8:111190216-111190266	AG04450	lung:	fetal
40	chr8:111190216-111190266	AoSMC	blood vessel:	n/a
41	chr8:111342449-111342499	T-47D	breast:	n/a
42	chr8:111342449-111342499	ProgFib	skin:	n/a
43	chr8:111342449-111342499	SK-N-SH	brain:	n/a
44	chr8:111214984-111215034	U87	brain:	n/a
45	chr8:111342449-111342499	ECC-1	luminal epithelium:	n/a
46	chr8:111214984-111215034	Jurkat	blood:	n/a
47	chr8:111342449-111342499	HRCEpiC	kidney:	n/a
48	chr8:111342449-111342499	HAEpiC	amniotic membrane:	n/a
49	chr8:111342449-111342499	PFSK-1	brain:	n/a
50	chr8:111214984-111215034	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:111170132..111173027-chr8:111181087..111182741,2	K562	blood:
2	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
3	chr8:111100909..111103732-chr8:111408499..111410564,2	K562	blood:
4	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
5	chr8:111148225..111150967-chr8:111837407..111839836,2	MCF-7	breast:
6	chr8:111246550..111249022-chr8:111251445..111253092,2	MCF-7	breast:
7	chr8:111314340..111317547-chr8:111319236..111321955,3	MCF-7	breast:
8	chr8:111147028..111149045-chr8:111188972..111191014,2	K562	blood:
9	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
10	chr8:111213386..111215697-chr8:111216006..111218910,2	MCF-7	breast:
11	chr8:111327454..111329140-chr8:111333315..111334824,2	MCF-7	breast:
12	chr8:111327454..111329140-chr8:111333315..111334824,2	MCF-7	breast:
13	chr8:90014072..90014862-chr8:111171720..111172332,2	MCF-7	breast:
14	chr8:111295797..111298136-chr8:111298202..111300823,3	MCF-7	breast:
15	chr8:111365137..111367407-chr8:111844337..111845381,8	MCF-7	breast:
16	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
17	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
18	chr8:100177691..100178432-chr8:111254768..111255288,2	MCF-7	breast:
19	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
20	chr8:111318905..111321198-chr8:111339196..111341691,2	MCF-7	breast:
21	chr8:111170132..111173027-chr8:111181087..111182741,2	K562	blood:
22	chr8:111318905..111321198-chr8:111339196..111341691,2	MCF-7	breast:
23	chr8:111213386..111215697-chr8:111216006..111218910,2	MCF-7	breast:
24	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
25	chr8:111319864..111321455-chr8:111321699..111324266,2	MCF-7	breast:
26	chr8:111295797..111298136-chr8:111298202..111300823,3	MCF-7	breast:
27	chr8:111147028..111149045-chr8:111188972..111191014,2	K562	blood:
28	chr8:111246550..111249022-chr8:111251445..111253092,2	MCF-7	breast:
29	chr8:111314340..111317547-chr8:111319236..111321955,3	MCF-7	breast:
30	chr8:111319864..111321455-chr8:111321699..111324266,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-1	chr8:111356682-111356824	ENSG00000253956
2	lnc-KCNV1-1	chr8:111361774-111361836	ENSG00000253956
3	lnc-KCNV1-1	chr8:111346972-111347538	ENSG00000253956

Variant related genes	Relation type
ENSG00000253956	TF binding region
ENSG00000253956	CpG island

Extended variants
information (count: 5630 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5630 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536174787	chr8:111131746-111131747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554606163	chr8:111131804-111131805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566637353	chr8:111131869-111131870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574691556	chr8:111131923-111131924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116063103	chr8:111131948-111131949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566296972	chr8:111131958-111131959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1868749	chr8:111132004-111132005	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs193065443	chr8:111132131-111132132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537379396	chr8:111132135-111132136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575347509	chr8:111132154-111132155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543857612	chr8:111132190-111132191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554586990	chr8:111132215-111132216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575166200	chr8:111132293-111132294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540898305	chr8:111132311-111132312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372277181	chr8:111132392-111132393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532709007	chr8:111132417-111132418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553653309	chr8:111132430-111132431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148966198	chr8:111132443-111132444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573498072	chr8:111132513-111132514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143709297	chr8:111132536-111132537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548273677	chr8:111132540-111132541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568468155	chr8:111132572-111132573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527695549	chr8:111132576-111132577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2084632	chr8:111132611-111132612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566433179	chr8:111132612-111132613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185296230	chr8:111132632-111132633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148093775	chr8:111132639-111132640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568845346	chr8:111132679-111132680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141830997	chr8:111132693-111132694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554387933	chr8:111132694-111132695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574448962	chr8:111132712-111132713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540239982	chr8:111132774-111132775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35843695	chr8:111132850-111132851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150379792	chr8:111132903-111132904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577658446	chr8:111132906-111132907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78689293	chr8:111132965-111132966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77166978	chr8:111132973-111132974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576936534	chr8:111132980-111132981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12680760	chr8:111132994-111132995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373200588	chr8:111133003-111133004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542275877	chr8:111133004-111133005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558741840	chr8:111133014-111133015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190588503	chr8:111133019-111133020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79774187	chr8:111133032-111133033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527632676	chr8:111133055-111133056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572505968	chr8:111133062-111133063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150137258	chr8:111133068-111133069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76182202	chr8:111133082-111133083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77676123	chr8:111133083-111133084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566423015	chr8:111133091-111133092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111130600-111132800	Enhancers	Adipose Nuclei	Adipose
2	chr8:111131000-111132000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:111132000-111133400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:111132800-111133600	Weak transcription	Adipose Nuclei	Adipose
5	chr8:111133400-111135400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:111133600-111134200	Enhancers	Adipose Nuclei	Adipose
7	chr8:111144400-111145800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:111145000-111145200	Enhancers	Fetal Brain Male	brain
9	chr8:111145000-111145400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:111145000-111145600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:111145000-111145600	Enhancers	Adipose Nuclei	Adipose
12	chr8:111145000-111145800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:111145000-111145800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:111145000-111145800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:111145200-111145400	Enhancers	Fetal Intestine Small	intestine
16	chr8:111145200-111145600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:111145200-111145600	Enhancers	Fetal Intestine Large	intestine
18	chr8:111145600-111147200	Weak transcription	Fetal Intestine Large	intestine
19	chr8:111147200-111148000	Enhancers	Fetal Intestine Small	intestine
20	chr8:111147200-111148600	Enhancers	Fetal Intestine Large	intestine
21	chr8:111148000-111150600	Weak transcription	Fetal Intestine Small	intestine
22	chr8:111150600-111150800	Enhancers	Fetal Intestine Small	intestine
23	chr8:111155200-111155600	Enhancers	Fetal Intestine Large	intestine
24	chr8:111155200-111155600	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr8:111166600-111167600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:111166600-111167600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:111166800-111167200	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr8:111166800-111168200	Enhancers	Fetal Intestine Large	intestine
29	chr8:111167000-111167200	Enhancers	Fetal Intestine Small	intestine
30	chr8:111167000-111168200	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr8:111167200-111172800	Weak transcription	Fetal Intestine Small	intestine
32	chr8:111168200-111172600	Weak transcription	Fetal Intestine Large	intestine
33	chr8:111168200-111173200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr8:111168400-111170600	Enhancers	HMEC	breast
35	chr8:111168600-111169200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr8:111168600-111169800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:111168800-111169800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr8:111168800-111169800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:111169000-111169800	Enhancers	NHEK	skin
40	chr8:111169200-111173400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:111169800-111173200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:111169800-111175800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:111170600-111173200	Weak transcription	HMEC	breast
44	chr8:111172600-111173400	Enhancers	Fetal Intestine Large	intestine
45	chr8:111172800-111174200	Enhancers	Fetal Intestine Small	intestine
46	chr8:111173200-111174200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:111173200-111174200	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr8:111173200-111175200	Enhancers	HMEC	breast
49	chr8:111173400-111174200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:111173400-111174200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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