Variant report

Variant	nsv831214
Chromosome Location	chr8:4498127-4679475
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	ATF1	chr8:4593306-4593480	K562	blood:	n/a	n/a
2	CEBPB	chr8:4499348-4499636	HepG2	liver:	n/a	chr8:4499487-4499498
3	CEBPB	chr8:4519375-4519607	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:4668991-4669179	HepG2	liver:	n/a	chr8:4669056-4669067
5	CEBPB	chr8:4520046-4520428	HepG2	liver:	n/a	chr8:4520233-4520242 chr8:4520233-4520242 chr8:4520232-4520243 chr8:4520233-4520242 chr8:4520231-4520244
6	CEBPB	chr8:4520057-4520407	Hela-S3	cervix:	n/a	chr8:4520233-4520242 chr8:4520233-4520242 chr8:4520232-4520243 chr8:4520233-4520242 chr8:4520231-4520244
7	CEBPB	chr8:4520053-4520398	K562	blood:	n/a	chr8:4520233-4520242 chr8:4520233-4520242 chr8:4520232-4520243 chr8:4520233-4520242 chr8:4520231-4520244
8	CEBPB	chr8:4520056-4520423	IMR90	lung:	n/a	chr8:4520233-4520242 chr8:4520233-4520242 chr8:4520232-4520243 chr8:4520233-4520242 chr8:4520231-4520244
9	CEBPB	chr8:4499408-4499621	A549	lung:	n/a	chr8:4499487-4499498
10	CEBPB	chr8:4548784-4549039	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:4613708-4613813	A549	lung:	n/a	n/a
12	CEBPB	chr8:4520063-4520415	A549	lung:	n/a	chr8:4520233-4520242 chr8:4520233-4520242 chr8:4520232-4520243 chr8:4520233-4520242 chr8:4520231-4520244
13	CEBPB	chr8:4520041-4520421	H1-hESC	embryonic stem cell:	n/a	chr8:4520233-4520242 chr8:4520233-4520242 chr8:4520232-4520243 chr8:4520233-4520242 chr8:4520231-4520244
14	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
15	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr8:4573370-4573868	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr8:4644672-4644761	GM13977	blood:	n/a	n/a
18	CTCF	chr8:4644700-4644850	GM12875	blood:	n/a	n/a
19	CTCF	chr8:4644660-4644810	GM12866	blood:	n/a	n/a
20	CTCF	chr8:4644660-4644810	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr8:4644540-4644690	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr8:4644600-4644750	GM12864	blood:	n/a	n/a
23	CTCF	chr8:4632207-4632286	Lung_OC	lung:	n/a	n/a
24	CTCF	chr8:4644700-4644850	GM12869	blood:	n/a	n/a
25	CTCF	chr8:4644600-4644750	HEK293	kidney:	n/a	n/a
26	CTCF	chr8:4573639-4573761	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
28	CTCF	chr8:4644640-4644790	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr8:4530539-4530582	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:4644600-4644750	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr8:4644640-4644790	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr8:4500740-4500890	GM06990	blood:	n/a	n/a
33	CTCF	chr8:4644660-4644810	GM12865	blood:	n/a	n/a
34	CTCF	chr8:4546760-4546910	HMF	breast:	n/a	n/a
35	CTCF	chr8:4644647-4644794	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
37	CTCF	chr8:4644600-4644750	GM12871	blood:	n/a	n/a
38	CTCF	chr8:4644658-4644814	Gliobla	brain:	n/a	n/a
39	CTCF	chr8:4644597-4644867	HepG2	liver:	n/a	n/a
40	CTCF	chr8:4644600-4644750	GM12872	blood:	n/a	n/a
41	CTCF	chr8:4644625-4644807	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr8:4644620-4644770	NB4	blood:	n/a	n/a
43	CTCF	chr8:4628455-4628505	LNCaP	prostate:	n/a	n/a
44	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
45	CTCF	chr8:4644600-4644750	SAEC	small airway:	n/a	n/a
46	CTCF	chr8:4644650-4644795	LNCaP	prostate:	n/a	n/a
47	CTCF	chr8:4644516-4644932	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:4644647-4644806	GM12891	blood:	n/a	n/a
49	CTCF	chr8:4644700-4644850	Caco-2	colon:	n/a	n/a
50	CTCF	chr8:4644587-4644847	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4504999-4505049	HMEC	breast:	n/a
2	chr8:4573688-4573738	NHBE	bronchial:	n/a
3	chr8:4601508-4601558	IMR90	lung:	fetal
4	chr8:4629524-4629574	Caco-2	colon:	n/a
5	chr8:4573688-4573738	Hela-S3	cervix:	n/a
6	chr8:4617087-4617137	SKMC	muscle:	n/a
7	chr8:4583386-4583436	NT2-D1	testis:	n/a
8	chr8:4573688-4573738	GM12891	blood:	n/a
9	chr8:4504944-4504994	HEK293	kidney:	embryo
10	chr8:4504999-4505049	SK-N-SH	brain:	n/a
11	chr8:4504944-4504994	MCF-7	breast:	n/a
12	chr8:4583355-4583405	Hepatocyte	liver:	n/a
13	chr8:4504944-4504994	SKMC	muscle:	n/a
14	chr8:4629524-4629574	AG04450	lung:	fetal
15	chr8:4601508-4601558	ovcar-3	ovarian:	n/a
16	chr8:4504848-4504898	MCF10A-Er-Src	breast:	n/a
17	chr8:4629524-4629574	AoSMC	blood vessel:	n/a
18	chr8:4601508-4601558	Hepatocyte	liver:	n/a
19	chr8:4637584-4637634	Hela-S3	cervix:	n/a
20	chr8:4573688-4573738	AoSMC	blood vessel:	n/a
21	chr8:4601579-4601629	GM12892	blood:	n/a
22	chr8:4573688-4573738	AG09309	skin:	n/a
23	chr8:4637584-4637634	HRCEpiC	kidney:	n/a
24	chr8:4617087-4617137	PrEC	prostate:	n/a
25	chr8:4504999-4505049	PFSK-1	brain:	n/a
26	chr8:4504848-4504898	SKMC	muscle:	n/a
27	chr8:4637584-4637634	HL-60	blood:	n/a
28	chr8:4637584-4637634	MCF-7	breast:	n/a
29	chr8:4629524-4629574	HRPEpiC	eye:	n/a
30	chr8:4644739-4644789	HRE	kidney:	n/a
31	chr8:4601508-4601558	NHDF-neo	bronchial:	n/a
32	chr8:4583386-4583436	PrEC	prostate:	n/a
33	chr8:4583386-4583436	LNCaP	prostate:	n/a
34	chr8:4504999-4505049	GM19239	blood:	n/a
35	chr8:4644739-4644789	A549	lung:	n/a
36	chr8:4601579-4601629	NHBE	bronchial:	n/a
37	chr8:4504944-4504994	AG09309	skin:	n/a
38	chr8:4583386-4583436	A549	lung:	n/a
39	chr8:4504848-4504898	BE2_C	brain:	n/a
40	chr8:4629524-4629574	SK-N-SH	brain:	n/a
41	chr8:4583355-4583405	BJ	skin:	n/a
42	chr8:4573688-4573738	Jurkat	blood:	n/a
43	chr8:4504848-4504898	HAEpiC	amniotic membrane:	n/a
44	chr8:4583355-4583405	T-47D	breast:	n/a
45	chr8:4583355-4583405	HNPCEpiC	eye:	n/a
46	chr8:4644739-4644789	Jurkat	blood:	n/a
47	chr8:4504944-4504994	SK-N-SH_RA	brain:	n/a
48	chr8:4644739-4644789	MCF10A-Er-Src	breast:	n/a
49	chr8:4601579-4601629	RPTEC	kidney:	n/a
50	chr8:4644719-4644769	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
2	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
3	chr8:4501243..4502892-chr8:4505644..4507988,2	K562	blood:
4	chr3:145223411..145224951-chr8:4505239..4506739,2	K562	blood:
5	chr2:220553002..220553652-chr8:4562250..4563228,2	HCT-116	colon:
6	chr8:4524296..4526779-chr8:4531992..4534283,2	K562	blood:
7	chr8:4524296..4526779-chr8:4531992..4534283,2	K562	blood:
8	chr8:4501243..4502892-chr8:4505644..4507988,2	K562	blood:
9	chr21:30519178..30519958-chr8:4582339..4582839,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-7	chr8:4644854-4646106	NONHSAT124751

Variant related genes	Relation type
PAICSP4	TF binding region
PAICSP4	CpG island

Extended variants
information (count: 10637 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:10637 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567754692	chr8:4498165-4498166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530587434	chr8:4498208-4498209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372228363	chr8:4498234-4498235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551315829	chr8:4498244-4498245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187110124	chr8:4498246-4498247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117991164	chr8:4498249-4498250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549493148	chr8:4498255-4498256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376778881	chr8:4498256-4498257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560576556	chr8:4498291-4498292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535183346	chr8:4498314-4498315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536692654	chr8:4498323-4498324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192439101	chr8:4498326-4498327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553297433	chr8:4498341-4498342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184575767	chr8:4498343-4498344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60059027	chr8:4498355-4498356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs201815251	chr8:4498385-4498386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569364028	chr8:4498399-4498400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74275224	chr8:4498401-4498402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58055126	chr8:4498402-4498403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187496750	chr8:4498408-4498409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575344247	chr8:4498413-4498414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372670606	chr8:4498436-4498437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147786564	chr8:4498437-4498438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554620063	chr8:4498471-4498472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572868151	chr8:4498484-4498485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193265686	chr8:4498495-4498496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564741471	chr8:4498540-4498541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185367150	chr8:4498560-4498561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141969306	chr8:4498571-4498572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141243571	chr8:4498577-4498578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149816804	chr8:4498584-4498585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369418525	chr8:4498618-4498619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370482128	chr8:4498620-4498621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530966697	chr8:4498647-4498648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189111366	chr8:4498650-4498651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567708686	chr8:4498663-4498664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77009850	chr8:4498671-4498672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547166506	chr8:4498678-4498679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558961245	chr8:4498684-4498685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544269591	chr8:4498700-4498701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181503665	chr8:4498705-4498706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539322954	chr8:4498707-4498708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77448767	chr8:4498741-4498742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375841445	chr8:4498748-4498749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145827059	chr8:4498763-4498764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534870456	chr8:4498766-4498767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184107945	chr8:4498787-4498788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188456310	chr8:4498789-4498790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79261092	chr8:4498806-4498807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533698140	chr8:4498807-4498808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4496600-4501400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:4497200-4498200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr8:4497600-4498200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:4497800-4498600	Weak transcription	Fetal Lung	lung
5	chr8:4498200-4499600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:4498200-4501400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:4498600-4501800	Enhancers	Fetal Lung	lung
8	chr8:4499600-4500200	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr8:4499600-4500200	Enhancers	Fetal Muscle Leg	muscle
10	chr8:4499600-4502000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr8:4500200-4501400	Weak transcription	Fetal Muscle Leg	muscle
12	chr8:4501400-4501600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:4501400-4501800	Enhancers	Fetal Muscle Leg	muscle
14	chr8:4501400-4502200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:4501600-4502000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:4501800-4502000	Enhancers	Fetal Kidney	kidney
17	chr8:4501800-4503000	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:4502000-4502400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr8:4502000-4503200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:4502400-4503200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:4502600-4502800	Enhancers	Fetal Kidney	kidney
22	chr8:4503000-4503200	Enhancers	Fetal Muscle Leg	muscle
23	chr8:4503200-4508800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr8:4508800-4510000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr8:4509600-4510600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:4510000-4510600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr8:4510000-4510600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:4510200-4510800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr8:4510600-4514400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr8:4511400-4511600	Enhancers	Adipose Nuclei	Adipose
31	chr8:4511600-4512000	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr8:4512000-4512200	Enhancers	Adipose Nuclei	Adipose
33	chr8:4514400-4514800	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:4514600-4515000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:4514600-4515000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:4514800-4515000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:4514800-4515400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:4515000-4518400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:4515200-4517000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:4517000-4517200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:4517200-4518600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:4518400-4518600	Enhancers	Fetal Brain Male	brain
43	chr8:4518400-4521200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:4518600-4521200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:4518800-4519200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:4518800-4520000	Weak transcription	Fetal Brain Male	brain
47	chr8:4518800-4520200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr8:4519000-4520000	Enhancers	Brain Germinal Matrix	brain
49	chr8:4519200-4520200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:4519400-4519800	Enhancers	Brain Angular Gyrus	brain

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