Variant report

Variant	nsv539644
Chromosome Location	chr8:69308665-69440129
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	BACH1	chr8:69423558-69423842	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:69339877-69339950	GM12878	blood:	n/a	n/a
3	BRCA1	chr8:69402913-69403106	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr8:69435102-69435144	GM12878	blood:	n/a	n/a
5	CBX3	chr8:69423313-69423576	K562	blood:	n/a	n/a
6	CEBPB	chr8:69346346-69346351	A549	lung:	n/a	n/a
7	CEBPB	chr8:69425561-69425885	A549	lung:	n/a	chr8:69425725-69425736
8	CEBPB	chr8:69399981-69400124	IMR90	lung:	n/a	chr8:69400026-69400037
9	CEBPB	chr8:69416056-69416415	MCF-7	breast:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
10	CEBPB	chr8:69416091-69416354	H1-hESC	embryonic stem cell:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
11	CEBPB	chr8:69425549-69425902	HepG2	liver:	n/a	chr8:69425725-69425736
12	CEBPB	chr8:69416086-69416408	HepG2	liver:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
13	CEBPB	chr8:69425534-69425937	MCF-7	breast:	n/a	chr8:69425725-69425736
14	CEBPB	chr8:69420081-69420248	HepG2	liver:	n/a	chr8:69420148-69420159
15	CEBPB	chr8:69425548-69425899	IMR90	lung:	n/a	chr8:69425725-69425736
16	CEBPB	chr8:69416060-69416366	K562	blood:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
17	CEBPB	chr8:69399911-69400117	HepG2	liver:	n/a	chr8:69400026-69400037
18	CEBPB	chr8:69425632-69425809	H1-hESC	embryonic stem cell:	n/a	chr8:69425725-69425736
19	CEBPB	chr8:69416096-69416415	Hela-S3	cervix:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
20	CEBPB	chr8:69416061-69416425	IMR90	lung:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
21	CEBPB	chr8:69420106-69420227	IMR90	lung:	n/a	chr8:69420148-69420159
22	CEBPB	chr8:69416145-69416406	A549	lung:	n/a	chr8:69416269-69416280 chr8:69416234-69416245
23	CEBPB	chr8:69425585-69425831	Hela-S3	cervix:	n/a	chr8:69425725-69425736
24	CEBPB	chr8:69399884-69400150	Hela-S3	cervix:	n/a	chr8:69400026-69400037
25	CHD2	chr8:69403081-69403123	GM12878	blood:	n/a	n/a
26	CTCF	chr8:69403020-69403170	HUVEC	blood vessel:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
27	CTCF	chr8:69344900-69345050	Caco-2	colon:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
28	CTCF	chr8:69402973-69403165	HepG2	liver:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
29	CTCF	chr8:69344860-69345010	Hela-S3	cervix:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
30	CTCF	chr8:69344920-69345070	AG04449	skin:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
31	CTCF	chr8:69344831-69345016	HepG2	liver:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
32	CTCF	chr8:69402965-69403238	HUVEC	blood vessel:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
33	CTCF	chr8:69402943-69403249	H1-hESC	embryonic stem cell:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
34	CTCF	chr8:69402953-69403211	A549	lung:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
35	CTCF	chr8:69344560-69344710	HFF	foreskin:	n/a	n/a
36	CTCF	chr8:69344900-69345050	HEEpiC	esophagus:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
37	CTCF	chr8:69344940-69345090	GM12865	blood:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
38	CTCF	chr8:69344851-69345032	HepG2	liver:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
39	CTCF	chr8:69344820-69344970	AG09319	gingival:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
40	CTCF	chr8:69344860-69345010	HEK293	kidney:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
41	CTCF	chr8:69403000-69403150	WERI-Rb-1	eye:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
42	CTCF	chr8:69344775-69345091	H1-hESC	embryonic stem cell:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953
43	CTCF	chr8:69402923-69403194	HepG2	liver:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
44	CTCF	chr8:69402947-69403216	Fibrobl	skin:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
45	CTCF	chr8:69402954-69403244	Medullo	brain:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
46	CTCF	chr8:69402941-69403234	MCF-7	breast:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
47	CTCF	chr8:69404160-69404310	HPF	lung:	n/a	n/a
48	CTCF	chr8:69402580-69402730	BJ	skin:	n/a	n/a
49	CTCF	chr8:69403000-69403150	GM12868	blood:	n/a	chr8:69403077-69403098 chr8:69403082-69403100
50	CTCF	chr8:69344860-69345010	GM12866	blood:	n/a	chr8:69344943-69344964 chr8:69344941-69344959 chr8:69344944-69344953

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:69355417-69355467	GM12892	blood:	n/a
2	chr8:69387218-69387268	MCF-7	breast:	n/a
3	chr8:69426081-69426131	PANC-1	pancreas:	n/a
4	chr8:69426081-69426131	HepG2	liver:	n/a
5	chr8:69387218-69387268	RPTEC	kidney:	n/a
6	chr8:69387218-69387268	GM12891	blood:	n/a
7	chr8:69348660-69348710	HCT-116	colon:	n/a
8	chr8:69387218-69387268	Hepatocyte	liver:	n/a
9	chr8:69355417-69355467	HMEC	breast:	n/a
10	chr8:69426081-69426131	A549	lung:	n/a
11	chr8:69350927-69350977	IMR90	lung:	fetal
12	chr8:69348660-69348710	NHDF-neo	bronchial:	n/a
13	chr8:69351585-69351635	HEEpiC	esophagus:	n/a
14	chr8:69350927-69350977	NH-A	brain:	n/a
15	chr8:69387218-69387268	AG09319	gingival:	n/a
16	chr8:69426081-69426131	HMEC	breast:	n/a
17	chr8:69350927-69350977	A549	lung:	n/a
18	chr8:69387218-69387268	HCT-116	colon:	n/a
19	chr8:69348660-69348710	HEEpiC	esophagus:	n/a
20	chr8:69348660-69348710	HNPCEpiC	eye:	n/a
21	chr8:69387218-69387268	AG04450	lung:	fetal
22	chr8:69351585-69351635	AG04450	lung:	fetal
23	chr8:69355417-69355467	SK-N-SH	brain:	n/a
24	chr8:69350927-69350977	AG10803	skin:	n/a
25	chr8:69387218-69387268	SK-N-MC	brain:	n/a
26	chr8:69351585-69351635	HRE	kidney:	n/a
27	chr8:69350927-69350977	HEK293	kidney:	embryo
28	chr8:69350927-69350977	HCT-116	colon:	n/a
29	chr8:69426081-69426131	H1-hESC	embryonic stem cell:	embryo
30	chr8:69355417-69355467	Hela-S3	cervix:	n/a
31	chr8:69387218-69387268	HMEC	breast:	n/a
32	chr8:69387218-69387268	SK-N-SH	brain:	n/a
33	chr8:69351585-69351635	Caco-2	colon:	n/a
34	chr8:69348660-69348710	PrEC	prostate:	n/a
35	chr8:69350927-69350977	AG09319	gingival:	n/a
36	chr8:69387218-69387268	HepG2	liver:	n/a
37	chr8:69387218-69387268	AG04449	skin:	fetal
38	chr8:69348660-69348710	GM12891	blood:	n/a
39	chr8:69355417-69355467	NB4	blood:	n/a
40	chr8:69355417-69355467	NHDF-neo	bronchial:	n/a
41	chr8:69350927-69350977	BE2_C	brain:	n/a
42	chr8:69348660-69348710	GM12878	blood:	n/a
43	chr8:69426081-69426131	ProgFib	skin:	n/a
44	chr8:69426081-69426131	HRPEpiC	eye:	n/a
45	chr8:69387218-69387268	NB4	blood:	n/a
46	chr8:69387218-69387268	GM19239	blood:	n/a
47	chr8:69355417-69355467	HNPCEpiC	eye:	n/a
48	chr8:69350927-69350977	PFSK-1	brain:	n/a
49	chr8:69351585-69351635	IMR90	lung:	fetal
50	chr8:69387218-69387268	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:69419792..69421543-chr8:69432398..69433901,2	MCF-7	breast:
2	chr2:209984149..209984947-chr8:69366893..69367419,2	MCF-7	breast:
3	chr8:69419792..69421543-chr8:69432398..69433901,2	MCF-7	breast:
4	chr8:69344569..69345547-chr8:69402811..69403513,3	MCF-7	breast:
5	chr8:69424228..69426143-chr8:69430126..69432077,2	MCF-7	breast:
6	chr8:69424228..69426143-chr8:69430126..69432077,2	MCF-7	breast:
7	chr8:69338439..69340713-chr8:69760510..69763451,2	MCF-7	breast:
8	chr8:69344569..69345547-chr8:69402811..69403513,3	MCF-7	breast:
9	chr8:69349497..69352271-chr8:69352394..69356040,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-664D7.4.1-6	chr8:69377026-69379303	ucscGeneNc_uc003xxw_1

Variant related genes	Relation type
C8orf34	TF binding region
RPS15AP25	TF binding region
C8orf34	CpG island
RPS15AP25	CpG island
ENSG00000165084	chromatin interactions

Extended variants
information (count: 3927 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3927 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189942932	chr8:69308670-69308671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544719127	chr8:69308672-69308673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73260728	chr8:69308695-69308696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536560577	chr8:69308725-69308726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73260731	chr8:69308777-69308778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182559883	chr8:69308789-69308790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372110763	chr8:69308806-69308807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187198216	chr8:69308834-69308835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550347671	chr8:69308855-69308856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563870893	chr8:69308863-69308864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61506473	chr8:69308920-69308921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56946858	chr8:69308969-69308970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60479864	chr8:69308976-69308977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532803118	chr8:69308990-69308991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1607142	chr8:69309001-69309002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565709170	chr8:69309048-69309049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35760127	chr8:69309078-69309079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555299326	chr8:69309105-69309106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1607143	chr8:69309142-69309143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs369681183	chr8:69309147-69309148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138464934	chr8:69309191-69309192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536087604	chr8:69309206-69309207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556314781	chr8:69309225-69309226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191959777	chr8:69309254-69309255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538877068	chr8:69309284-69309285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143108183	chr8:69309293-69309294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145928063	chr8:69309294-69309295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4346979	chr8:69309305-69309306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs554753734	chr8:69309318-69309319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574578885	chr8:69309320-69309321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556970665	chr8:69309323-69309324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573973736	chr8:69309336-69309337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13252745	chr8:69309408-69309409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs369533601	chr8:69309541-69309542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563859249	chr8:69309562-69309563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185145170	chr8:69309642-69309643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546443107	chr8:69309753-69309754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559604582	chr8:69309808-69309809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528494400	chr8:69309913-69309914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548173953	chr8:69309921-69309922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576523157	chr8:69309974-69309975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371387664	chr8:69309996-69309997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188811431	chr8:69310034-69310035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530994621	chr8:69310051-69310052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575129923	chr8:69310054-69310055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193069825	chr8:69310086-69310087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9298133	chr8:69310100-69310101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs538570812	chr8:69310122-69310123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558925470	chr8:69310131-69310132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543842445	chr8:69310171-69310172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	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
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69308200-69312200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:69312200-69312800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:69312800-69313000	Enhancers	Lung	lung
4	chr8:69312800-69313800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:69313000-69314200	Weak transcription	Lung	lung
6	chr8:69313800-69314000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:69317200-69342600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:69319400-69319800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:69320800-69321000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:69321000-69324000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:69321400-69322400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:69322000-69322400	Enhancers	NHEK	skin
13	chr8:69324000-69324200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:69324200-69325800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:69325000-69325200	ZNF genes & repeats	Aorta	Aorta
16	chr8:69325200-69332400	Weak transcription	Aorta	Aorta
17	chr8:69325800-69326200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:69332400-69332600	Enhancers	Aorta	Aorta
19	chr8:69332600-69333000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr8:69332600-69333800	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr8:69332600-69334000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:69332600-69334200	Weak transcription	Aorta	Aorta
23	chr8:69333000-69333400	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr8:69333000-69334000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr8:69333000-69334000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:69333000-69334000	Enhancers	HUVEC	blood vessel
27	chr8:69333000-69334000	Enhancers	NHEK	skin
28	chr8:69333200-69333600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:69333200-69333800	Enhancers	NH-A	brain
30	chr8:69333400-69334200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr8:69333400-69334200	Enhancers	HMEC	breast
32	chr8:69333600-69334200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:69334200-69334400	Enhancers	Aorta	Aorta
34	chr8:69334400-69335000	Weak transcription	Aorta	Aorta
35	chr8:69340800-69341600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:69341600-69342200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:69342200-69343800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:69342600-69343000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr8:69342800-69364800	Weak transcription	Aorta	Aorta
40	chr8:69343000-69345600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:69345800-69346000	Enhancers	Adipose Nuclei	Adipose
42	chr8:69345800-69346200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr8:69346000-69360000	Weak transcription	Adipose Nuclei	Adipose
44	chr8:69350800-69354000	Weak transcription	Brain Anterior Caudate	brain
45	chr8:69351600-69353800	Weak transcription	Fetal Brain Male	brain
46	chr8:69353200-69362000	Weak transcription	Pancreas	Pancrea
47	chr8:69358600-69359000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:69359000-69371800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:69365200-69365600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:69365600-69369600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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