Variant report

Variant	esv2759613
Chromosome Location	chr8:50873293-51137995
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	ATF2	chr8:50969058-50969384	GM12878	blood:	n/a	n/a
2	ATF2	chr8:50968957-50969420	GM12878	blood:	n/a	n/a
3	BACH1	chr8:50892249-50892339	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:50969021-50969265	GM12878	blood:	n/a	n/a
5	BATF	chr8:51057978-51058142	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:50969022-50969362	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:50969028-50969333	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:50969028-50969399	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:51038532-51038842	GM12878	blood:	n/a	chr8:51038771-51038792
10	BRCA1	chr8:50873303-50873331	HepG2	liver:	n/a	n/a
11	BRCA1	chr8:50968793-50969924	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr8:50999011-50999073	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:50915138-50915395	HepG2	liver:	n/a	chr8:50915245-50915256 chr8:50915245-50915258 chr8:50915245-50915258
14	CEBPB	chr8:51031956-51032118	HepG2	liver:	n/a	chr8:51032029-51032040 chr8:51032027-51032044
15	CEBPB	chr8:50952445-50952812	IMR90	lung:	n/a	chr8:50952625-50952636 chr8:50952624-50952641 chr8:50952625-50952638
16	CEBPB	chr8:50952484-50952781	A549	lung:	n/a	chr8:50952625-50952636 chr8:50952624-50952641 chr8:50952625-50952638
17	CEBPB	chr8:50898826-50899188	IMR90	lung:	n/a	chr8:50899007-50899018 chr8:50899008-50899017 chr8:50899006-50899019 chr8:50899006-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899006-50899019
18	CEBPB	chr8:50952411-50952877	A549	lung:	n/a	chr8:50952625-50952636 chr8:50952624-50952641 chr8:50952625-50952638
19	CEBPB	chr8:50886882-50887168	HepG2	liver:	n/a	chr8:50887017-50887028
20	CEBPB	chr8:50892514-50892801	H1-hESC	embryonic stem cell:	n/a	chr8:50892652-50892663
21	CEBPB	chr8:50901060-50901243	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:50980388-50980486	K562	blood:	n/a	n/a
23	CEBPB	chr8:50958472-50958923	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:50998909-50999173	HepG2	liver:	n/a	chr8:50999014-50999025
25	CEBPB	chr8:50886853-50887178	A549	lung:	n/a	chr8:50887017-50887028
26	CEBPB	chr8:50898832-50899174	A549	lung:	n/a	chr8:50899007-50899018 chr8:50899008-50899017 chr8:50899006-50899019 chr8:50899006-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899006-50899019
27	CEBPB	chr8:50995529-50996028	HepG2	liver:	n/a	chr8:50995945-50995958 chr8:50995947-50995958 chr8:50995945-50995958 chr8:50995677-50995688
28	CEBPB	chr8:50998901-50999139	A549	lung:	n/a	chr8:50999014-50999025
29	CEBPB	chr8:50892506-50892785	A549	lung:	n/a	chr8:50892652-50892663
30	CEBPB	chr8:51137953-51138297	IMR90	lung:	n/a	chr8:51138124-51138135
31	CEBPB	chr8:51052157-51052994	IMR90	lung:	n/a	chr8:51052494-51052505
32	CEBPB	chr8:51013566-51013832	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:51056460-51056606	A549	lung:	n/a	n/a
34	CEBPB	chr8:50946696-50947071	Hela-S3	cervix:	n/a	chr8:50946882-50946893
35	CEBPB	chr8:50946710-50947079	IMR90	lung:	n/a	chr8:50946882-50946893
36	CEBPB	chr8:50892563-50892820	MCF-7	breast:	n/a	chr8:50892652-50892663
37	CEBPB	chr8:50946736-50947055	HepG2	liver:	n/a	chr8:50946882-50946893
38	CEBPB	chr8:50966647-50966977	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:50995520-50996068	IMR90	lung:	n/a	chr8:50995945-50995958 chr8:50995947-50995958 chr8:50995945-50995958 chr8:50995677-50995688
40	CEBPB	chr8:50898917-50899117	H1-hESC	embryonic stem cell:	n/a	chr8:50899007-50899018 chr8:50899008-50899017 chr8:50899006-50899019 chr8:50899006-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899006-50899019
41	CEBPB	chr8:51013564-51013854	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:50898821-50899173	HepG2	liver:	n/a	chr8:50899007-50899018 chr8:50899008-50899017 chr8:50899006-50899019 chr8:50899006-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899006-50899019
43	CEBPB	chr8:50946776-50946987	A549	lung:	n/a	chr8:50946882-50946893
44	CEBPB	chr8:50997447-50997787	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr8:51039822-51040220	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:50898862-50899156	K562	blood:	n/a	chr8:50899007-50899018 chr8:50899008-50899017 chr8:50899006-50899019 chr8:50899006-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899006-50899019
47	CEBPB	chr8:50915122-50915357	A549	lung:	n/a	chr8:50915245-50915256 chr8:50915245-50915258 chr8:50915245-50915258
48	CEBPB	chr8:50886852-50887236	Hela-S3	cervix:	n/a	chr8:50887017-50887028
49	CEBPB	chr8:51052112-51052647	Hela-S3	cervix:	n/a	chr8:51052494-51052505
50	CEBPB	chr8:50941263-50941546	IMR90	lung:	n/a	chr8:50941381-50941392

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:50875600-50875650	IMR90	lung:	fetal
2	chr8:50875600-50875650	IMR90	lung:	fetal
3	chr8:50980859-50980909	HepG2	liver:	n/a
4	chr8:50947399-50947449	NH-A	brain:	n/a
5	chr8:51039471-51039521	HepG2	liver:	n/a
6	chr8:50891848-50891898	SK-N-SH_RA	brain:	n/a
7	chr8:51039471-51039521	AG10803	skin:	n/a
8	chr8:50904638-50904688	BE2_C	brain:	n/a
9	chr8:50968578-50968628	BJ	skin:	n/a
10	chr8:50904638-50904688	CMK	blood:	n/a
11	chr8:50891864-50891914	ECC-1	luminal epithelium:	n/a
12	chr8:51095593-51095643	U87	brain:	n/a
13	chr8:50904638-50904688	AG04450	lung:	fetal
14	chr8:50968578-50968628	SK-N-SH_RA	brain:	n/a
15	chr8:50891848-50891898	NB4	blood:	n/a
16	chr8:50891848-50891898	HCF	heart:	n/a
17	chr8:50892702-50892752	MCF10A-Er-Src	breast:	n/a
18	chr8:51039471-51039521	PFSK-1	brain:	n/a
19	chr8:50947399-50947449	AG09319	gingival:	n/a
20	chr8:51095593-51095643	BE2_C	brain:	n/a
21	chr8:50980859-50980909	ovcar-3	ovarian:	n/a
22	chr8:50891848-50891898	SAEC	small airway:	n/a
23	chr8:50875600-50875650	SK-N-SH	brain:	n/a
24	chr8:50875600-50875650	ovcar-3	ovarian:	n/a
25	chr8:51039471-51039521	HRCEpiC	kidney:	n/a
26	chr8:50891864-50891914	NT2-D1	testis:	n/a
27	chr8:50904638-50904688	PANC-1	pancreas:	n/a
28	chr8:50891767-50891817	AoSMC	blood vessel:	n/a
29	chr8:50891848-50891898	IMR90	lung:	fetal
30	chr8:51039471-51039521	SKMC	muscle:	n/a
31	chr8:50892702-50892752	HNPCEpiC	eye:	n/a
32	chr8:50891848-50891898	SKMC	muscle:	n/a
33	chr8:50891848-50891898	NT2-D1	testis:	n/a
34	chr8:50891767-50891817	CMK	blood:	n/a
35	chr8:50968578-50968628	CMK	blood:	n/a
36	chr8:50891848-50891898	GM12891	blood:	n/a
37	chr8:51095593-51095643	ProgFib	skin:	n/a
38	chr8:50891767-50891817	Hela-S3	cervix:	n/a
39	chr8:51039471-51039521	AG04449	skin:	fetal
40	chr8:50891848-50891898	HCPEpiC	choroid plexus:	n/a
41	chr8:50968578-50968628	NHDF-neo	bronchial:	n/a
42	chr8:50904638-50904688	MCF10A-Er-Src	breast:	n/a
43	chr8:50891864-50891914	HCPEpiC	choroid plexus:	n/a
44	chr8:50891864-50891914	PrEC	prostate:	n/a
45	chr8:50968578-50968628	PFSK-1	brain:	n/a
46	chr8:50891848-50891898	AoSMC	blood vessel:	n/a
47	chr8:50891848-50891898	ProgFib	skin:	n/a
48	chr8:50892893-50892943	Jurkat	blood:	n/a
49	chr8:51095593-51095643	GM12892	blood:	n/a
50	chr8:50891864-50891914	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:51050537..51053146-chr8:51056966..51059260,2	K562	blood:
2	chr8:50925829..50927969-chr8:50932438..50935189,2	MCF-7	breast:
3	chr8:50906818..50909515-chr8:50916418..50918690,2	K562	blood:
4	chr8:50988839..50990732-chr8:50993883..50996257,2	K562	blood:
5	chr8:50925829..50927969-chr8:50932438..50935189,2	MCF-7	breast:
6	chr8:50709168..50710848-chr8:50931158..50933465,2	MCF-7	breast:
7	chr8:51030711..51032424-chr8:51036929..51039858,2	MCF-7	breast:
8	chr8:50861606..50863840-chr8:50871624..50874600,2	MCF-7	breast:
9	chr8:50906818..50909515-chr8:50916418..50918690,2	K562	blood:
10	chr8:51050537..51053146-chr8:51056966..51059260,2	K562	blood:
11	chr8:50988839..50990732-chr8:50993883..50996257,2	K562	blood:
12	chr8:50947214..50948091-chr8:51310516..51311364,3	MCF-7	breast:
13	chr8:50947077..50947745-chr8:51310573..51311162,2	MCF-7	breast:
14	chr8:51030711..51032424-chr8:51036929..51039858,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-15	chr8:51085121-51085195	NONHSAT126524
2	lnc-C8orf22-14	chr8:51076059-51076529	NONHSAT126523

Variant related genes	Relation type
SNTG1	TF binding region
SNTG1	CpG island

Extended variants
information (count: 7939 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:7939 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2015043	chr8:50873293-50873294	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554984013	chr8:50873316-50873317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372624611	chr8:50873322-50873323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572749929	chr8:50873340-50873341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540241709	chr8:50873347-50873348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147942502	chr8:50873349-50873350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193250750	chr8:50873360-50873361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532240098	chr8:50873367-50873368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2860009	chr8:50873406-50873407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185718198	chr8:50873410-50873411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562690710	chr8:50873442-50873443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529866080	chr8:50873456-50873457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189302401	chr8:50873482-50873483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141740123	chr8:50873525-50873526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180901085	chr8:50873537-50873538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10441571	chr8:50873608-50873609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147116303	chr8:50873647-50873648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571355460	chr8:50873718-50873719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6988557	chr8:50873729-50873730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs573620442	chr8:50873759-50873760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs67415969	chr8:50873843-50873844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs374023650	chr8:50873849-50873850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569404360	chr8:50873856-50873857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs67856006	chr8:50873860-50873861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185603773	chr8:50873895-50873896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368161717	chr8:50873932-50873933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188749970	chr8:50873952-50873953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540971800	chr8:50873963-50873964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573096991	chr8:50874052-50874053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558563625	chr8:50874071-50874072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539867976	chr8:50874117-50874118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545333010	chr8:50874125-50874126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10441546	chr8:50874135-50874136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544263538	chr8:50874151-50874152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565367894	chr8:50874168-50874169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565219723	chr8:50874172-50874173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181377296	chr8:50874184-50874185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541669335	chr8:50874185-50874186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560336486	chr8:50874188-50874189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544272071	chr8:50874191-50874192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs318893	chr8:50874200-50874201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs552081741	chr8:50874217-50874218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571273218	chr8:50874279-50874280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13266609	chr8:50874280-50874281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs16914099	chr8:50874313-50874314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551486607	chr8:50874341-50874342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561444880	chr8:50874465-50874466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530094062	chr8:50874475-50874476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114619700	chr8:50874479-50874480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548491438	chr8:50874505-50874506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50855200-50875200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:50860400-50875400	Weak transcription	Fetal Intestine Small	intestine
3	chr8:50869800-50875000	Weak transcription	Fetal Brain Male	brain
4	chr8:50870200-50875400	Weak transcription	Fetal Lung	lung
5	chr8:50870400-50875400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:50870400-50875600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:50871000-50874600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:50872800-50875400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:50873200-50873400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:50873200-50873400	Enhancers	Brain Germinal Matrix	brain
11	chr8:50873400-50874400	Weak transcription	Brain Germinal Matrix	brain
12	chr8:50874400-50874800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr8:50874400-50876200	Enhancers	Brain Germinal Matrix	brain
14	chr8:50874600-50874800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:50874600-50875600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:50874800-50876000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr8:50875000-50876000	Enhancers	Fetal Brain Male	brain
18	chr8:50875000-50876000	Enhancers	Fetal Brain Female	brain
19	chr8:50875200-50876000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:50875400-50875800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:50875400-50876000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:50875400-50876000	Enhancers	Fetal Intestine Small	intestine
23	chr8:50875400-50876200	Enhancers	Fetal Intestine Large	intestine
24	chr8:50875400-50876200	Enhancers	Fetal Stomach	stomach
25	chr8:50875400-50876600	Enhancers	Fetal Lung	lung
26	chr8:50875600-50876000	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr8:50875600-50876800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:50875600-50876800	Enhancers	Hela-S3	cervix
29	chr8:50875600-50877000	Enhancers	Ovary	ovary
30	chr8:50875800-50882800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:50876000-50878400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr8:50876000-50889200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr8:50878200-50878400	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr8:50878400-50882400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr8:50882400-50883000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr8:50882600-50883400	Enhancers	Fetal Brain Female	brain
37	chr8:50887000-50887600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:50887600-50890000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:50889200-50889600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr8:50889400-50889800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr8:50889600-50892000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr8:50889800-50890800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr8:50890000-50890200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:50890200-50893600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:50890800-50891000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr8:50890800-50891200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr8:50891600-50892400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:50891800-50892400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:50892000-50894000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr8:50892200-50892600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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