Variant report

Variant	nsv1034771
Chromosome Location	chr8:3969767-4255716
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	chr8:4101087-4101507	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:4049134-4049669	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:4107408-4107727	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:3982138-3982421	GM12878	blood:	n/a	chr8:3982277-3982285 chr8:3982247-3982258
5	BATF	chr8:3982135-3982323	GM12878	blood:	n/a	chr8:3982277-3982285 chr8:3982247-3982258
6	BHLHE40	chr8:4092217-4092221	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:4060102-4060103	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:4026526-4026926	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:4080738-4080739	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:4130382-4130659	K562	blood:	n/a	chr8:4130518-4130529
11	CEBPB	chr8:4031696-4031915	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:4015758-4016093	A549	lung:	n/a	n/a
13	CEBPB	chr8:4081697-4082074	IMR90	lung:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
14	CEBPB	chr8:4081643-4082076	A549	lung:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
15	CEBPB	chr8:4019605-4019772	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:4127248-4127571	IMR90	lung:	n/a	chr8:4127386-4127399 chr8:4127386-4127397
17	CEBPB	chr8:4081771-4082062	ECC-1	luminal epithelium:	n/a	chr8:4081879-4081890
18	CEBPB	chr8:4227126-4227302	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:4167514-4167871	H1-hESC	embryonic stem cell:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
20	CEBPB	chr8:4242430-4242568	A549	lung:	n/a	n/a
21	CEBPB	chr8:4214721-4214989	HepG2	liver:	n/a	chr8:4214850-4214859 chr8:4214850-4214859 chr8:4214850-4214859
22	CEBPB	chr8:4167517-4167869	HepG2	liver:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
23	CEBPB	chr8:4193140-4193359	HepG2	liver:	n/a	chr8:4193194-4193205 chr8:4193194-4193207
24	CEBPB	chr8:4227032-4227320	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:4002172-4002414	A549	lung:	n/a	chr8:4002319-4002330
26	CEBPB	chr8:4102669-4102952	H1-hESC	embryonic stem cell:	n/a	chr8:4102773-4102784
27	CEBPB	chr8:4127206-4127570	HepG2	liver:	n/a	chr8:4127386-4127399 chr8:4127386-4127397
28	CEBPB	chr8:4002146-4002495	HepG2	liver:	n/a	chr8:4002319-4002330
29	CEBPB	chr8:4015769-4016050	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:4130359-4130708	IMR90	lung:	n/a	chr8:4130518-4130529
31	CEBPB	chr8:4130370-4130681	HepG2	liver:	n/a	chr8:4130518-4130529
32	CEBPB	chr8:3977406-3977473	K562	blood:	n/a	n/a
33	CEBPB	chr8:4150042-4150242	HepG2	liver:	n/a	chr8:4150160-4150171
34	CEBPB	chr8:4015775-4016105	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:4081771-4081978	A549	lung:	n/a	chr8:4081879-4081890
36	CEBPB	chr8:4081697-4082078	HepG2	liver:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719
37	CEBPB	chr8:4031786-4031957	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr8:3977236-3977429	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:3981268-3981579	IMR90	lung:	n/a	chr8:3981423-3981434 chr8:3981421-3981434 chr8:3981421-3981432
40	CEBPB	chr8:4167533-4167842	IMR90	lung:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
41	CEBPB	chr8:3981312-3981555	A549	lung:	n/a	chr8:3981423-3981434 chr8:3981421-3981434 chr8:3981421-3981432
42	CEBPB	chr8:4130358-4130684	H1-hESC	embryonic stem cell:	n/a	chr8:4130518-4130529
43	CEBPB	chr8:4250895-4251106	HepG2	liver:	n/a	chr8:4250917-4250928
44	CEBPB	chr8:4081798-4082075	ECC-1	luminal epithelium:	n/a	chr8:4081879-4081890
45	CEBPB	chr8:4102603-4102944	A549	lung:	n/a	chr8:4102773-4102784
46	CEBPB	chr8:4130385-4130669	A549	lung:	n/a	chr8:4130518-4130529
47	CEBPB	chr8:3981319-3981552	HepG2	liver:	n/a	chr8:3981423-3981434 chr8:3981421-3981434 chr8:3981421-3981432
48	CEBPB	chr8:4002286-4002430	H1-hESC	embryonic stem cell:	n/a	chr8:4002319-4002330
49	CEBPB	chr8:4167594-4167820	K562	blood:	n/a	chr8:4167683-4167694 chr8:4167680-4167697
50	CEBPB	chr8:4081702-4082079	H1-hESC	embryonic stem cell:	n/a	chr8:4081879-4081890 chr8:4081708-4081719 chr8:4081708-4081719

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:3982537-3982587	Hepatocyte	liver:	n/a
2	chr8:3982537-3982587	Hepatocyte	liver:	n/a
3	chr8:4183726-4183776	HRE	kidney:	n/a
4	chr8:4183726-4183776	SK-N-SH_RA	brain:	n/a
5	chr8:3974798-3974848	HIPEpiC	eye:	n/a
6	chr8:4183880-4183930	HAEpiC	amniotic membrane:	n/a
7	chr8:3974030-3974080	ECC-1	luminal epithelium:	n/a
8	chr8:3982599-3982649	NT2-D1	testis:	n/a
9	chr8:3974030-3974080	Hepatocyte	liver:	n/a
10	chr8:4188646-4188696	NHDF-neo	bronchial:	n/a
11	chr8:3970118-3970168	AG04449	skin:	fetal
12	chr8:3982599-3982649	GM12892	blood:	n/a
13	chr8:4188646-4188696	IMR90	lung:	fetal
14	chr8:3974030-3974080	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:3974030-3974080	AG09319	gingival:	n/a
16	chr8:3974934-3974984	HCM	heart:	n/a
17	chr8:3974145-3974195	AG04449	skin:	fetal
18	chr8:3982599-3982649	K562	blood:	n/a
19	chr8:4183880-4183930	Hela-S3	cervix:	n/a
20	chr8:3974225-3974275	GM06990	blood:	n/a
21	chr8:3974934-3974984	HepG2	liver:	n/a
22	chr8:3974030-3974080	HCM	heart:	n/a
23	chr8:3974798-3974848	Hela-S3	cervix:	n/a
24	chr8:4183726-4183776	HCT-116	colon:	n/a
25	chr8:3974145-3974195	HCT-116	colon:	n/a
26	chr8:3970118-3970168	PrEC	prostate:	n/a
27	chr8:3974798-3974848	GM19239	blood:	n/a
28	chr8:3970118-3970168	MCF-7	breast:	n/a
29	chr8:4183642-4183692	NHBE	bronchial:	n/a
30	chr8:3974145-3974195	SKMC	muscle:	n/a
31	chr8:4238976-4239026	HepG2	liver:	n/a
32	chr8:4238976-4239026	AG04449	skin:	fetal
33	chr8:4183726-4183776	ECC-1	luminal epithelium:	n/a
34	chr8:3974145-3974195	PrEC	prostate:	n/a
35	chr8:3974225-3974275	AG04450	lung:	fetal
36	chr8:3982537-3982587	HEEpiC	esophagus:	n/a
37	chr8:4238976-4239026	PANC-1	pancreas:	n/a
38	chr8:3983001-3983051	K562	blood:	n/a
39	chr8:3974225-3974275	HCT-116	colon:	n/a
40	chr8:3974030-3974080	LNCaP	prostate:	n/a
41	chr8:3974145-3974195	K562	blood:	n/a
42	chr8:3974145-3974195	HAEpiC	amniotic membrane:	n/a
43	chr8:3970118-3970168	NT2-D1	testis:	n/a
44	chr8:3974798-3974848	SK-N-MC	brain:	n/a
45	chr8:3974225-3974275	ovcar-3	ovarian:	n/a
46	chr8:3982599-3982649	HRCEpiC	kidney:	n/a
47	chr8:4183726-4183776	AoSMC	blood vessel:	n/a
48	chr8:3974030-3974080	AG04449	skin:	fetal
49	chr8:3974225-3974275	SK-N-MC	brain:	n/a
50	chr8:4183726-4183776	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:4010079..4014350-chr8:4015920..4018884,3	K562	blood:
2	chr8:4091951..4092554-chr8:4399113..4400010,2	MCF-7	breast:
3	chr8:4010079..4014350-chr8:4015920..4018884,3	K562	blood:
4	chr1:103323089..103325462-chr8:4135925..4138695,2	MCF-7	breast:
5	chr8:4138578..4139163-chr8:4399169..4399679,2	MCF-7	breast:
6	chr8:4091582..4092324-chr8:4399511..4400398,2	MCF-7	breast:
7	chr8:4010079..4014350-chr8:4015920..4019883,4	K562	blood:
8	chr8:4092133..4092721-chr8:4257157..4257997,2	MCF-7	breast:
9	chr8:4010079..4014350-chr8:4015920..4019883,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-8	chr8:4250344-4250612	NONHSAT124750

Variant related genes	Relation type
RN7SL872P	TF binding region
RN7SL872P	CpG island

Extended variants
information (count: 11058 )
Associated
traits (count: 134 )

Variant overlapped rSNPs/rCNVs (count:11058 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533650198	chr8:3969783-3969784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140417420	chr8:3969819-3969820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556435300	chr8:3969820-3969821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574364138	chr8:3969831-3969832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185629034	chr8:3969835-3969836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566724385	chr8:3969849-3969850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559682678	chr8:3969865-3969866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190153866	chr8:3969906-3969907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545930977	chr8:3969910-3969911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564003642	chr8:3969930-3969931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541428627	chr8:3969932-3969933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181858229	chr8:3969945-3969946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115436836	chr8:3969952-3969953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562407663	chr8:3969958-3969959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529570816	chr8:3969966-3969967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548099288	chr8:3969977-3969978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76774317	chr8:3969985-3969986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184846341	chr8:3969998-3969999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560125800	chr8:3970011-3970012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551883553	chr8:3970015-3970016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570016033	chr8:3970019-3970020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538068949	chr8:3970022-3970023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556039595	chr8:3970027-3970028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574404356	chr8:3970045-3970046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535403322	chr8:3970056-3970057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369954998	chr8:3970060-3970061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188855060	chr8:3970065-3970066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181292212	chr8:3970067-3970068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149866000	chr8:3970079-3970080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536161028	chr8:3970094-3970095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144904832	chr8:3970100-3970101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564224186	chr8:3970116-3970117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576007117	chr8:3970119-3970120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149050527	chr8:3970125-3970126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7015737	chr8:3970138-3970139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs115293148	chr8:3970145-3970146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185154052	chr8:3970148-3970149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143066947	chr8:3970175-3970176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533378994	chr8:3970202-3970203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376977067	chr8:3970221-3970222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570139837	chr8:3970233-3970234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7827749	chr8:3970268-3970269	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138771388	chr8:3970270-3970271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189910968	chr8:3970275-3970276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182275210	chr8:3970285-3970286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142527375	chr8:3970288-3970289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538093401	chr8:3970295-3970296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565604973	chr8:3970298-3970299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557918983	chr8:3970304-3970305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530400512	chr8:3970308-3970309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:134)

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
Pancreatic ductal adenocarcinoma	19077451	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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	22315472	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3966800-3971000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:3971000-3972200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
3	chr8:3980000-3980200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:3980200-3980400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:3980400-3980600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:3980400-3981600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:3980600-3981600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:3980600-3983200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:3981200-3981400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr8:3981400-3983400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr8:3981600-3981800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:3981600-3982800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr8:3981600-3984400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr8:3981600-3984400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:3981600-3984600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:3981800-3982000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr8:3981800-3982200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr8:3981800-3984400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:3981800-3984600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:3981800-3993800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr8:3982000-3983000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr8:3982000-3984600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr8:3982200-3984400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr8:3982800-3984400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:3983000-3984200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:3983200-3983400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:3983200-3983600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:3983200-3983600	Enhancers	Fetal Kidney	kidney
29	chr8:3983400-3983800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr8:3983600-3984000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr8:3983800-3984200	Enhancers	Pancreas	Pancrea
32	chr8:3983800-3984800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr8:3984400-3985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr8:3984600-3985600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr8:3985400-3985600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr8:3985600-3985800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr8:3993800-3994800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:3993800-3994800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:3994000-3994600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:3994000-3994800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:3994000-3994800	Enhancers	Brain Germinal Matrix	brain
42	chr8:3994800-3999800	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr8:3997000-3997200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:3999800-4000000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr8:4000000-4001200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr8:4001200-4001800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:4001400-4001600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:4001400-4001800	Enhancers	Fetal Lung	lung
49	chr8:4010800-4011000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:4010800-4011400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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