Variant report

Variant	nsv831391
Chromosome Location	chr8:92578256-92761091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:184)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 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	ATF1	chr8:92674288-92674429	K562	blood:	n/a	n/a
2	ATF2	chr8:92732457-92732756	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:92680042-92680176	K562	blood:	n/a	n/a
4	BCL11A	chr8:92732468-92732788	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:92674375-92674595	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:92732565-92732741	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr8:92696035-92696258	K562	blood:	n/a	n/a
8	CCNT2	chr8:92674172-92674533	K562	blood:	n/a	n/a
9	CEBPB	chr8:92590435-92590574	HepG2	liver:	n/a	chr8:92590478-92590489
10	CEBPB	chr8:92674370-92674533	K562	blood:	n/a	n/a
11	CEBPB	chr8:92592125-92592132	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:92680363-92680502	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:92750990-92751077	HepG2	liver:	n/a	chr8:92751012-92751029
14	CEBPB	chr8:92729708-92729912	HepG2	liver:	n/a	chr8:92729850-92729861
15	CEBPB	chr8:92590382-92590582	A549	lung:	n/a	chr8:92590478-92590489
16	CEBPB	chr8:92653863-92654142	A549	lung:	n/a	chr8:92653971-92653982
17	CEBPB	chr8:92729709-92729897	A549	lung:	n/a	chr8:92729850-92729861
18	CEBPB	chr8:92613691-92614012	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:92592693-92592879	A549	lung:	n/a	n/a
20	CEBPB	chr8:92668382-92668439	K562	blood:	n/a	chr8:92668407-92668416
21	CEBPB	chr8:92653968-92653998	H1-hESC	embryonic stem cell:	n/a	chr8:92653971-92653982
22	CEBPB	chr8:92612572-92612964	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:92638287-92638408	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:92646108-92646384	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:92641799-92642004	HepG2	liver:	n/a	chr8:92641959-92641970
26	CEBPB	chr8:92729697-92730038	MCF-7	breast:	n/a	chr8:92729850-92729861
27	CEBPB	chr8:92624753-92625186	MCF-7	breast:	n/a	n/a
28	CEBPB	chr8:92653849-92654105	HepG2	liver:	n/a	chr8:92653971-92653982
29	CHD1	chr8:92613065-92613954	IMR90	lung:	n/a	n/a
30	CHD2	chr8:92732509-92732815	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:92670500-92670650	RPTEC	kidney:	n/a	chr8:92670579-92670600
32	CTCF	chr8:92670800-92670950	RPTEC	kidney:	n/a	n/a
33	CTCF	chr8:92670540-92670690	AG04449	skin:	n/a	chr8:92670579-92670600
34	CTCF	chr8:92675740-92675890	BJ	skin:	n/a	n/a
35	CTCF	chr8:92675766-92675863	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr8:92670540-92670690	BJ	skin:	n/a	chr8:92670579-92670600
37	CTCF	chr8:92620561-92620759	Medullo	brain:	n/a	n/a
38	CTCF	chr8:92651220-92651370	AG10803	skin:	n/a	chr8:92651282-92651300
39	CTCF	chr8:92675813-92675846	GM12891	blood:	n/a	n/a
40	CTCF	chr8:92609220-92609370	HCT-116	colon:	n/a	chr8:92609343-92609351
41	CTCF	chr8:92670500-92670650	HPAF	blood vessel:	n/a	chr8:92670579-92670600
42	CTCF	chr8:92609240-92609390	WERI-Rb-1	eye:	n/a	chr8:92609343-92609351
43	CTCF	chr8:92670460-92670610	GM12872	blood:	n/a	chr8:92670579-92670600
44	CTCF	chr8:92670500-92670650	AG10803	skin:	n/a	chr8:92670579-92670600
45	CTCF	chr8:92670612-92670619	ProgFib	skin:	n/a	n/a
46	CTCF	chr8:92609280-92609430	RPTEC	kidney:	n/a	chr8:92609343-92609351
47	CTCF	chr8:92695020-92695072	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:92675820-92675970	HFF	foreskin:	n/a	n/a
49	CTCF	chr8:92735820-92735970	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr8:92651240-92651390	RPTEC	kidney:	n/a	chr8:92651282-92651300

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:92622592-92622642	PANC-1	pancreas:	n/a
2	chr8:92622592-92622642	PANC-1	pancreas:	n/a
3	chr8:92647788-92647838	HRE	kidney:	n/a
4	chr8:92611305-92611355	HNPCEpiC	eye:	n/a
5	chr8:92647788-92647838	HEK293	kidney:	embryo
6	chr8:92647788-92647838	GM06990	blood:	n/a
7	chr8:92611305-92611355	BE2_C	brain:	n/a
8	chr8:92611305-92611355	HEK293	kidney:	embryo
9	chr8:92611305-92611355	NB4	blood:	n/a
10	chr8:92622592-92622642	HepG2	liver:	n/a
11	chr8:92647788-92647838	BE2_C	brain:	n/a
12	chr8:92611305-92611355	AoSMC	blood vessel:	n/a
13	chr8:92611305-92611355	BJ	skin:	n/a
14	chr8:92611305-92611355	HAEpiC	amniotic membrane:	n/a
15	chr8:92647788-92647838	NH-A	brain:	n/a
16	chr8:92622592-92622642	HMEC	breast:	n/a
17	chr8:92611305-92611355	GM06990	blood:	n/a
18	chr8:92622592-92622642	HRPEpiC	eye:	n/a
19	chr8:92611305-92611355	PrEC	prostate:	n/a
20	chr8:92611305-92611355	NHBE	bronchial:	n/a
21	chr8:92647788-92647838	GM19239	blood:	n/a
22	chr8:92611305-92611355	Caco-2	colon:	n/a
23	chr8:92611305-92611355	AG04450	lung:	fetal
24	chr8:92622592-92622642	AG10803	skin:	n/a
25	chr8:92647788-92647838	SAEC	small airway:	n/a
26	chr8:92611305-92611355	SK-N-MC	brain:	n/a
27	chr8:92611305-92611355	SKMC	muscle:	n/a
28	chr8:92622592-92622642	NT2-D1	testis:	n/a
29	chr8:92611305-92611355	HRPEpiC	eye:	n/a
30	chr8:92622592-92622642	ProgFib	skin:	n/a
31	chr8:92647788-92647838	NB4	blood:	n/a
32	chr8:92647788-92647838	NHDF-neo	bronchial:	n/a
33	chr8:92647788-92647838	SK-N-MC	brain:	n/a
34	chr8:92611305-92611355	U87	brain:	n/a
35	chr8:92622592-92622642	T-47D	breast:	n/a
36	chr8:92611305-92611355	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:92647788-92647838	ECC-1	luminal epithelium:	n/a
38	chr8:92611305-92611355	NH-A	brain:	n/a
39	chr8:92622592-92622642	ovcar-3	ovarian:	n/a
40	chr8:92611305-92611355	SAEC	small airway:	n/a
41	chr8:92647788-92647838	PANC-1	pancreas:	n/a
42	chr8:92622592-92622642	BE2_C	brain:	n/a
43	chr8:92611305-92611355	HUVEC	blood vessel:	n/a
44	chr8:92611305-92611355	AG09319	gingival:	n/a
45	chr8:92622592-92622642	NH-A	brain:	n/a
46	chr8:92647788-92647838	AG04449	skin:	fetal
47	chr8:92622592-92622642	K562	blood:	n/a
48	chr8:92622592-92622642	HRCEpiC	kidney:	n/a
49	chr8:92622592-92622642	Hela-S3	cervix:	n/a
50	chr8:92647788-92647838	BJ	skin:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:92611694..92613502-chr8:92613647..92615230,2	K562	blood:
2	chr12:61057349..61058143-chr8:92718418..92719083,2	MCF-7	breast:
3	chr13:52025318..52028013-chr8:92725864..92728504,2	MCF-7	breast:
4	chr8:92609898..92611827-chr8:92612731..92615308,2	MCF-7	breast:
5	chr8:92638061..92640011-chr8:92644229..92646416,2	MCF-7	breast:
6	chr8:92624289..92626072-chr8:92628158..92630578,2	MCF-7	breast:
7	chr8:92609898..92611827-chr8:92612731..92615308,2	MCF-7	breast:
8	chr8:92624289..92626072-chr8:92628158..92630578,2	MCF-7	breast:
9	chr8:92640658..92644497-chr8:92645172..92649601,4	MCF-7	breast:
10	chr8:92640658..92644497-chr8:92645172..92649601,4	MCF-7	breast:
11	chr8:92589301..92592290-chr8:92598286..92600105,2	MCF-7	breast:
12	chr8:92467413..92468365-chr8:92670147..92671073,3	MCF-7	breast:
13	chr8:92637072..92640837-chr8:92642560..92645637,4	K562	blood:
14	chr8:92589301..92592290-chr8:92598286..92600105,2	MCF-7	breast:
15	chr8:92636432..92639157-chr8:92654180..92656409,2	MCF-7	breast:
16	chr8:92637072..92640837-chr8:92642560..92645637,4	K562	blood:
17	chr8:92693140..92695604-chr8:92697839..92699430,2	K562	blood:
18	chr8:92693140..92695604-chr8:92697839..92699430,2	K562	blood:
19	chr8:92636432..92639157-chr8:92654180..92656409,2	MCF-7	breast:
20	chr8:92638061..92640011-chr8:92644229..92646416,2	MCF-7	breast:
21	chr8:92611694..92613502-chr8:92613647..92615230,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC26A7-2	chr8:92607193-92607469	NONHSAT127680

No data

Variant related genes	Relation type
RN7SKP231	TF binding region
RN7SKP231	CpG island
ENSG00000236778	chromatin interactions
ENSG00000102786	chromatin interactions

Extended variants
information (count: 2779 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:2779 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534423745	chr8:92586828-92586829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183204044	chr8:92586849-92586850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540717913	chr8:92586882-92586883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7832321	chr8:92586901-92586902	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs574281985	chr8:92586968-92586969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538205085	chr8:92586971-92586972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188170010	chr8:92587033-92587034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578097068	chr8:92587062-92587063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148202436	chr8:92587081-92587082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560590616	chr8:92587089-92587090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572237006	chr8:92587132-92587133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542816083	chr8:92587172-92587173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558879521	chr8:92587217-92587218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115077702	chr8:92587331-92587332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531630567	chr8:92587342-92587343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549846098	chr8:92587349-92587350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550399721	chr8:92589227-92589228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74741004	chr8:92589281-92589282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78693550	chr8:92589283-92589284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571916320	chr8:92589299-92589300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532843865	chr8:92589368-92589369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148936471	chr8:92589423-92589424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566041664	chr8:92589461-92589462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536270111	chr8:92589465-92589466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs56160120	chr8:92589513-92589514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs142819501	chr8:92589561-92589562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537198262	chr8:92589594-92589595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552696298	chr8:92590021-92590022	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs574343669	chr8:92590022-92590023	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs192710521	chr8:92590024-92590025	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs548039914	chr8:92590037-92590038	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs566256742	chr8:92590109-92590110	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs112731726	chr8:92590118-92590119	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs35840034	chr8:92590137-92590138	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs78117890	chr8:92590160-92590161	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs184891361	chr8:92590191-92590192	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs535787647	chr8:92590476-92590477	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs369019561	chr8:92590546-92590547	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs556673710	chr8:92590587-92590588	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs190969078	chr8:92605275-92605276	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs138724059	chr8:92605319-92605320	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573025093	chr8:92605321-92605322	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs540424171	chr8:92605323-92605324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561902320	chr8:92605330-92605331	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs141902593	chr8:92605356-92605357	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs181735193	chr8:92605369-92605370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs562476937	chr8:92605377-92605378	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs527757239	chr8:92605450-92605451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs1457052	chr8:92605773-92605774	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs6988467	chr8:92605781-92605782	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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
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
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
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92586800-92587400	Enhancers	Fetal Heart	heart
2	chr8:92589200-92589600	Enhancers	Fetal Brain Male	brain
3	chr8:92590000-92590200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:92590400-92590600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
5	chr8:92607200-92607400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:92607200-92607600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:92607200-92607800	Enhancers	NHDF-Ad	bronchial
8	chr8:92607600-92609200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:92607800-92609000	Weak transcription	NHDF-Ad	bronchial
10	chr8:92609000-92611600	Enhancers	NHDF-Ad	bronchial
11	chr8:92609200-92609400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:92609200-92609400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:92609200-92612200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:92609200-92612200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:92609400-92611600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:92609400-92611800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:92609600-92614400	Enhancers	NHLF	lung
18	chr8:92610000-92612400	Enhancers	Fetal Brain Male	brain
19	chr8:92610200-92612200	Enhancers	NH-A	brain
20	chr8:92610200-92614400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:92610400-92610800	Enhancers	Fetal Brain Female	brain
22	chr8:92610400-92613600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:92610600-92612800	Enhancers	Fetal Stomach	stomach
24	chr8:92610600-92613000	Enhancers	Fetal Lung	lung
25	chr8:92610600-92613600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:92610800-92612200	Weak transcription	Fetal Brain Female	brain
27	chr8:92611200-92612200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:92611200-92612800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr8:92611400-92612600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:92611400-92614200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:92611400-92614200	Enhancers	HSMMtube	muscle
32	chr8:92611600-92612000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr8:92611600-92612800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:92611600-92613000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:92611600-92613000	Enhancers	Colon Smooth Muscle	Colon
36	chr8:92611600-92613200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr8:92611600-92613400	Flanking Active TSS	NHDF-Ad	bronchial
38	chr8:92611600-92614200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr8:92611600-92614200	Enhancers	HSMM	muscle
40	chr8:92611800-92614000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr8:92612000-92612400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr8:92612000-92612800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:92612200-92612600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:92612200-92612600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:92612200-92612800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:92612200-92612800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:92612200-92612800	Enhancers	Fetal Brain Female	brain
48	chr8:92612200-92612800	Enhancers	Ovary	ovary
49	chr8:92612200-92612800	Enhancers	Rectal Smooth Muscle	rectum
50	chr8:92612200-92612800	Enhancers	Stomach Smooth Muscle	stomach

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