Variant report

Variant	esv2759621
Chromosome Location	chr8:63156123-63260182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:1220)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:63162335-63162587	HepG2	liver:	n/a	n/a
2	BACH1	chr8:63162004-63162082	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:63253812-63253906	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:63235596-63235772	K562	blood:	n/a	n/a
5	BACH1	chr8:63161254-63161272	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr8:63183164-63183338	A549	lung:	n/a	chr8:63183190-63183201
7	CEBPB	chr8:63250304-63250633	IMR90	lung:	n/a	chr8:63250473-63250482 chr8:63250471-63250482 chr8:63250473-63250484
8	CEBPB	chr8:63221103-63221158	H1-hESC	embryonic stem cell:	n/a	chr8:63221110-63221121
9	CEBPB	chr8:63183084-63183498	IMR90	lung:	n/a	chr8:63183190-63183201
10	CEBPB	chr8:63250300-63250644	HepG2	liver:	n/a	chr8:63250473-63250482 chr8:63250471-63250482 chr8:63250473-63250484
11	CEBPB	chr8:63183037-63183410	HepG2	liver:	n/a	chr8:63183190-63183201
12	CEBPB	chr8:63162998-63163340	A549	lung:	n/a	chr8:63163165-63163178 chr8:63163167-63163178
13	CEBPB	chr8:63220959-63221300	IMR90	lung:	n/a	chr8:63221110-63221121
14	CEBPB	chr8:63220967-63221275	HepG2	liver:	n/a	chr8:63221110-63221121
15	CEBPB	chr8:63220993-63221284	K562	blood:	n/a	chr8:63221110-63221121
16	CEBPB	chr8:63162970-63163351	Hela-S3	cervix:	n/a	chr8:63163165-63163178 chr8:63163167-63163178
17	CEBPB	chr8:63250302-63250589	A549	lung:	n/a	chr8:63250473-63250482 chr8:63250471-63250482 chr8:63250473-63250484
18	CEBPB	chr8:63183152-63183291	H1-hESC	embryonic stem cell:	n/a	chr8:63183190-63183201
19	CEBPB	chr8:63220940-63221270	A549	lung:	n/a	chr8:63221110-63221121
20	CHD1	chr8:63161096-63161206	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr8:63162467-63162593	HepG2	liver:	n/a	n/a
22	CHD2	chr8:63161665-63162207	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr8:63160560-63160730	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:63206439-63206605	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr8:63161387-63161992	A549	lung:	n/a	n/a
26	CTBP2	chr8:63160517-63162469	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:63157660-63157810	HRE	kidney:	n/a	n/a
28	CTCF	chr8:63160629-63160748	SK-N-SH_RA	brain:	n/a	chr8:63160696-63160705
29	CTCF	chr8:63167909-63168057	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:63157740-63157890	HAc	cerebellar:	n/a	n/a
31	CTCF	chr8:63157640-63157790	HMEC	breast:	n/a	n/a
32	CTCF	chr8:63167920-63168070	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr8:63160600-63160750	HRPEpiC	eye:	n/a	chr8:63160696-63160705
34	CTCF	chr8:63167860-63168010	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr8:63157620-63157770	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr8:63167900-63168050	HMEC	breast:	n/a	n/a
37	CTCF	chr8:63167900-63168050	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr8:63160620-63160770	HBMEC	blood vessel:	n/a	chr8:63160696-63160705
39	CTCF	chr8:63167920-63168070	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr8:63160640-63160759	Fibrobl	skin:	n/a	chr8:63160696-63160705
41	CTCF	chr8:63160600-63160750	HCFaa	heart:	n/a	chr8:63160696-63160705
42	CTCF	chr8:63157700-63157850	HFF	foreskin:	n/a	n/a
43	CTCF	chr8:63157680-63157830	NB4	blood:	n/a	n/a
44	CTCF	chr8:63160600-63160750	HEK293	kidney:	n/a	chr8:63160696-63160705
45	CTCF	chr8:63167900-63168050	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:63160640-63160790	NHDF-neo	bronchial:	n/a	chr8:63160696-63160705
47	CTCF	chr8:63157740-63157782	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr8:63167920-63168070	A549	lung:	n/a	n/a
49	CTCF	chr8:63157680-63157830	GM12872	blood:	n/a	n/a
50	CTCF	chr8:63157648-63157834	Hela-S3	cervix:	n/a	n/a

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63160127-63160177	HL-60	blood:	n/a
2	chr8:63160761-63160811	NHBE	bronchial:	n/a
3	chr8:63161616-63161666	NHDF-neo	bronchial:	n/a
4	chr8:63161676-63161726	PANC-1	pancreas:	n/a
5	chr8:63160256-63160306	MCF-7	breast:	n/a
6	chr8:63160333-63160383	AoSMC	blood vessel:	n/a
7	chr8:63161609-63161659	GM12878	blood:	n/a
8	chr8:63160256-63160306	GM19239	blood:	n/a
9	chr8:63161609-63161659	PFSK-1	brain:	n/a
10	chr8:63160761-63160811	HRCEpiC	kidney:	n/a
11	chr8:63160282-63160332	MCF-7	breast:	n/a
12	chr8:63158463-63158513	Jurkat	blood:	n/a
13	chr8:63161676-63161726	HCT-116	colon:	n/a
14	chr8:63160417-63160467	MCF10A-Er-Src	breast:	n/a
15	chr8:63161609-63161659	SK-N-SH	brain:	n/a
16	chr8:63160256-63160306	HL-60	blood:	n/a
17	chr8:63160853-63160903	MCF10A-Er-Src	breast:	n/a
18	chr8:63162277-63162327	HCPEpiC	choroid plexus:	n/a
19	chr8:63160127-63160177	AoSMC	blood vessel:	n/a
20	chr8:63161077-63161127	SK-N-SH	brain:	n/a
21	chr8:63158463-63158513	AG04450	lung:	fetal
22	chr8:63161579-63161629	ovcar-3	ovarian:	n/a
23	chr8:63161077-63161127	HEK293	kidney:	embryo
24	chr8:63160509-63160559	NT2-D1	testis:	n/a
25	chr8:63161077-63161127	HUVEC	blood vessel:	n/a
26	chr8:63160853-63160903	HCT-116	colon:	n/a
27	chr8:63160761-63160811	GM12878	blood:	n/a
28	chr8:63160282-63160332	AG04450	lung:	fetal
29	chr8:63160256-63160306	A549	lung:	n/a
30	chr8:63162277-63162327	BJ	skin:	n/a
31	chr8:63161579-63161629	NHBE	bronchial:	n/a
32	chr8:63160256-63160306	HRPEpiC	eye:	n/a
33	chr8:63161589-63161639	NHBE	bronchial:	n/a
34	chr8:63160853-63160903	BE2_C	brain:	n/a
35	chr8:63161609-63161659	SAEC	small airway:	n/a
36	chr8:63160761-63160811	CMK	blood:	n/a
37	chr8:63160761-63160811	SK-N-SH	brain:	n/a
38	chr8:63160746-63160796	K562	blood:	n/a
39	chr8:63160333-63160383	HepG2	liver:	n/a
40	chr8:63160853-63160903	HL-60	blood:	n/a
41	chr8:63160127-63160177	HIPEpiC	eye:	n/a
42	chr8:63161589-63161639	K562	blood:	n/a
43	chr8:63161077-63161127	GM19239	blood:	n/a
44	chr8:63160333-63160383	HCT-116	colon:	n/a
45	chr8:63160417-63160467	Jurkat	blood:	n/a
46	chr8:63161077-63161127	HNPCEpiC	eye:	n/a
47	chr8:63164796-63164846	HRPEpiC	eye:	n/a
48	chr8:63161616-63161666	LNCaP	prostate:	n/a
49	chr8:63161589-63161639	AoSMC	blood vessel:	n/a
50	chr8:63160417-63160467	HCPEpiC	choroid plexus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:63181507..63183694-chr8:63186121..63188039,2	K562	blood:
2	chr8:63173073..63176211-chr8:63176262..63178420,3	K562	blood:
3	chr8:63181507..63183694-chr8:63186121..63188039,2	K562	blood:
4	chr8:63157703..63161119-chr8:63165423..63168636,3	K562	blood:
5	chr8:63157703..63161119-chr8:63165423..63168636,3	K562	blood:
6	chr8:63163914..63166859-chr8:63167989..63170549,2	MCF-7	breast:
7	chr8:63171900..63174465-chr8:63951289..63953516,2	K562	blood:
8	chr8:63175758..63177483-chr8:63180388..63182096,2	K562	blood:
9	chr8:63163914..63166859-chr8:63167989..63170549,2	MCF-7	breast:
10	chr8:63175758..63177483-chr8:63180388..63182096,2	K562	blood:
11	chr8:63173073..63176211-chr8:63176262..63178420,3	K562	blood:

No data

Variant related genes	Relation type
NKAIN3	TF binding region
NKAIN3	CpG island
ENSG00000137563	chromatin interactions

Extended variants
information (count: 3635 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3635 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1384681	chr8:63156123-63156124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369920522	chr8:63156149-63156150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555196992	chr8:63156176-63156177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187010249	chr8:63156203-63156204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35321426	chr8:63156247-63156248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562694770	chr8:63156263-63156264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556083241	chr8:63156264-63156265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578250779	chr8:63156302-63156303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148126571	chr8:63156311-63156312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141836997	chr8:63156312-63156313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546644083	chr8:63156354-63156355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572711941	chr8:63156356-63156357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75018175	chr8:63156406-63156407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561249018	chr8:63156444-63156445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531798860	chr8:63156449-63156450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532130927	chr8:63156450-63156451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552327590	chr8:63156477-63156478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12676617	chr8:63156512-63156513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188765433	chr8:63156522-63156523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564892505	chr8:63156565-63156566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532371018	chr8:63156579-63156580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376316195	chr8:63156596-63156597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182039407	chr8:63156610-63156611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566404715	chr8:63156657-63156658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10957214	chr8:63156658-63156659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs13250501	chr8:63156678-63156679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34299696	chr8:63156686-63156687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs397951932	chr8:63156703-63156704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376299987	chr8:63156704-63156705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146244070	chr8:63156705-63156706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368558359	chr8:63156713-63156714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79378965	chr8:63156743-63156744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567258514	chr8:63156753-63156754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537898896	chr8:63156762-63156763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10957215	chr8:63156797-63156798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs10957216	chr8:63156813-63156814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538622826	chr8:63156846-63156847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79145002	chr8:63156901-63156902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186226347	chr8:63156906-63156907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs60718882	chr8:63156930-63156931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs55997675	chr8:63157002-63157003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs2625409	chr8:63157015-63157016	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs533269399	chr8:63157098-63157099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189857189	chr8:63157126-63157127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576466105	chr8:63157139-63157140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536796787	chr8:63157145-63157146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386726118	chr8:63157222-63157223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78035258	chr8:63157223-63157224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532395230	chr8:63157244-63157245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143751776	chr8:63157280-63157281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Salivary gland tumor	18059337	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63154200-63159400	Weak transcription	Fetal Brain Male	brain
2	chr8:63155400-63160600	Weak transcription	Pancreas	Pancrea
3	chr8:63157800-63158000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:63158200-63159400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:63158400-63158800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:63158400-63159400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:63158600-63159000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:63158600-63159200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr8:63158600-63159600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:63158600-63159800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr8:63158800-63159000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
12	chr8:63158800-63159000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr8:63158800-63159000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:63158800-63159000	Enhancers	Brain Germinal Matrix	brain
15	chr8:63158800-63159400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
16	chr8:63158800-63160000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr8:63159000-63159200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr8:63159000-63159200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr8:63159000-63159200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
20	chr8:63159000-63159400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:63159000-63159400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr8:63159000-63159600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr8:63159000-63159800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
24	chr8:63159000-63160000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr8:63159000-63160400	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr8:63159200-63159400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr8:63159200-63159800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr8:63159200-63160000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr8:63159200-63160000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
30	chr8:63159200-63160000	Enhancers	A549	lung
31	chr8:63159200-63163800	Active TSS	Fetal Brain Female	brain
32	chr8:63159400-63159600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr8:63159400-63159600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr8:63159400-63159800	Enhancers	Fetal Brain Male	brain
35	chr8:63159400-63160000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:63159400-63160200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr8:63159600-63159800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
38	chr8:63159600-63159800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:63159600-63160000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
40	chr8:63159600-63160000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:63159600-63160000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:63159600-63160000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr8:63159600-63160000	Bivalent Enhancer	Fetal Intestine Large	intestine
44	chr8:63159600-63160000	Enhancers	Fetal Stomach	stomach
45	chr8:63159600-63160200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:63159600-63160200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr8:63159600-63160200	Flanking Active TSS	Fetal Kidney	kidney
48	chr8:63159600-63161600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
49	chr8:63159600-63162800	Active TSS	Brain Anterior Caudate	brain
50	chr8:63159800-63160000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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