Variant report

Variant	nsv1034230
Chromosome Location	chr6:65579061-65887750
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	CEBPB	chr6:65655361-65655722	A549	lung:	n/a	n/a
2	CEBPB	chr6:65716699-65717038	H1-hESC	embryonic stem cell:	n/a	chr6:65716874-65716885
3	CEBPB	chr6:65655359-65655621	MCF-7	breast:	n/a	n/a
4	CEBPB	chr6:65769840-65770057	HepG2	liver:	n/a	chr6:65769968-65769979
5	CEBPB	chr6:65755724-65756051	K562	blood:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
6	CEBPB	chr6:65655375-65655700	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:65688032-65688232	A549	lung:	n/a	chr6:65688100-65688111
8	CEBPB	chr6:65867011-65867264	K562	blood:	n/a	n/a
9	CEBPB	chr6:65681969-65682239	HepG2	liver:	n/a	chr6:65682126-65682137 chr6:65682100-65682111
10	CEBPB	chr6:65694841-65695250	Hela-S3	cervix:	n/a	chr6:65695020-65695031
11	CEBPB	chr6:65714814-65714999	A549	lung:	n/a	chr6:65714880-65714891
12	CEBPB	chr6:65866950-65867272	IMR90	lung:	n/a	n/a
13	CEBPB	chr6:65678779-65679145	HepG2	liver:	n/a	chr6:65678958-65678969 chr6:65678960-65678971
14	CEBPB	chr6:65678779-65679107	IMR90	lung:	n/a	chr6:65678958-65678969 chr6:65678960-65678971
15	CEBPB	chr6:65678825-65679127	H1-hESC	embryonic stem cell:	n/a	chr6:65678958-65678969 chr6:65678960-65678971
16	CEBPB	chr6:65675755-65676074	IMR90	lung:	n/a	chr6:65675924-65675933
17	CEBPB	chr6:65600236-65601065	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:65675891-65675987	Hela-S3	cervix:	n/a	chr6:65675924-65675933
19	CEBPB	chr6:65687931-65688253	HepG2	liver:	n/a	chr6:65688100-65688111
20	CEBPB	chr6:65678799-65679086	A549	lung:	n/a	chr6:65678958-65678969 chr6:65678960-65678971
21	CEBPB	chr6:65867884-65868178	IMR90	lung:	n/a	chr6:65867989-65868002 chr6:65867991-65868000 chr6:65867991-65868002
22	CEBPB	chr6:65694879-65695194	HepG2	liver:	n/a	chr6:65695020-65695031
23	CEBPB	chr6:65716700-65717039	HepG2	liver:	n/a	chr6:65716874-65716885
24	CEBPB	chr6:65675819-65675920	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:65757460-65757715	HepG2	liver:	n/a	chr6:65757602-65757613
26	CEBPB	chr6:65694902-65695171	H1-hESC	embryonic stem cell:	n/a	chr6:65695020-65695031
27	CEBPB	chr6:65613037-65613385	HepG2	liver:	n/a	chr6:65613217-65613226 chr6:65613217-65613228 chr6:65613215-65613228
28	CEBPB	chr6:65675810-65676027	HepG2	liver:	n/a	chr6:65675924-65675933
29	CEBPB	chr6:65755702-65756077	Hela-S3	cervix:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
30	CEBPB	chr6:65625912-65626201	HepG2	liver:	n/a	chr6:65626064-65626077 chr6:65626064-65626075 chr6:65626064-65626077 chr6:65626066-65626077
31	CEBPB	chr6:65623864-65624542	MCF-7	breast:	n/a	chr6:65624191-65624204
32	CEBPB	chr6:65877133-65877402	HepG2	liver:	n/a	chr6:65877288-65877299
33	CEBPB	chr6:65655287-65655751	MCF-7	breast:	n/a	n/a
34	CEBPB	chr6:65655365-65655724	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:65655435-65655701	K562	blood:	n/a	n/a
36	CEBPB	chr6:65852457-65852466	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:65655355-65655724	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:65866932-65867276	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:65755777-65756072	A549	lung:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
40	CEBPB	chr6:65655382-65655691	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:65866986-65867268	A549	lung:	n/a	n/a
42	CEBPB	chr6:65866943-65867264	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:65755716-65756078	HepG2	liver:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
44	CEBPB	chr6:65600382-65600740	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:65624048-65624422	MCF-7	breast:	n/a	chr6:65624191-65624204
46	CEBPB	chr6:65714828-65715032	HepG2	liver:	n/a	chr6:65714880-65714891
47	CEBPB	chr6:65840033-65840285	HepG2	liver:	n/a	chr6:65840147-65840158
48	CEBPB	chr6:65755738-65756070	IMR90	lung:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
49	CEBPB	chr6:65623734-65624686	Hela-S3	cervix:	n/a	chr6:65624191-65624204
50	CEBPB	chr6:65675769-65676009	A549	lung:	n/a	chr6:65675924-65675933

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:65779514-65779564	ECC-1	luminal epithelium:	n/a
2	chr6:65779514-65779564	ECC-1	luminal epithelium:	n/a
3	chr6:65779514-65779564	LNCaP	prostate:	n/a
4	chr6:65779514-65779564	AoSMC	blood vessel:	n/a
5	chr6:65779514-65779564	HRPEpiC	eye:	n/a
6	chr6:65779514-65779564	Hepatocyte	liver:	n/a
7	chr6:65779514-65779564	PFSK-1	brain:	n/a
8	chr6:65779514-65779564	HIPEpiC	eye:	n/a
9	chr6:65779514-65779564	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:65779514-65779564	HCM	heart:	n/a
11	chr6:65779514-65779564	H1-hESC	embryonic stem cell:	embryo
12	chr6:65779514-65779564	GM19239	blood:	n/a
13	chr6:65779514-65779564	NB4	blood:	n/a
14	chr6:65779514-65779564	SKMC	muscle:	n/a
15	chr6:65779514-65779564	HAEpiC	amniotic membrane:	n/a
16	chr6:65779514-65779564	NHDF-neo	bronchial:	n/a
17	chr6:65779514-65779564	HMEC	breast:	n/a
18	chr6:65779514-65779564	GM12892	blood:	n/a
19	chr6:65779514-65779564	AG04450	lung:	fetal
20	chr6:65779514-65779564	HUVEC	blood vessel:	n/a
21	chr6:65779514-65779564	HepG2	liver:	n/a
22	chr6:65779514-65779564	BJ	skin:	n/a
23	chr6:65779514-65779564	GM12878	blood:	n/a
24	chr6:65779514-65779564	SK-N-MC	brain:	n/a
25	chr6:65779514-65779564	ovcar-3	ovarian:	n/a
26	chr6:65779514-65779564	BE2_C	brain:	n/a
27	chr6:65779514-65779564	HCF	heart:	n/a
28	chr6:65779514-65779564	MCF10A-Er-Src	breast:	n/a
29	chr6:65779514-65779564	Caco-2	colon:	n/a
30	chr6:65779514-65779564	HNPCEpiC	eye:	n/a
31	chr6:65779514-65779564	ProgFib	skin:	n/a
32	chr6:65779514-65779564	K562	blood:	n/a
33	chr6:65779514-65779564	SK-N-SH_RA	brain:	n/a
34	chr6:65779514-65779564	NHBE	bronchial:	n/a
35	chr6:65779514-65779564	HCT-116	colon:	n/a
36	chr6:65779514-65779564	HL-60	blood:	n/a
37	chr6:65779514-65779564	SAEC	small airway:	n/a
38	chr6:65779514-65779564	A549	lung:	n/a
39	chr6:65779514-65779564	Hela-S3	cervix:	n/a
40	chr6:65779514-65779564	GM06990	blood:	n/a
41	chr6:65779514-65779564	T-47D	breast:	n/a
42	chr6:65779514-65779564	PrEC	prostate:	n/a
43	chr6:65779514-65779564	HEK293	kidney:	embryo
44	chr6:65779514-65779564	AG04449	skin:	fetal
45	chr6:65779514-65779564	MCF-7	breast:	n/a
46	chr6:65779514-65779564	AG10803	skin:	n/a
47	chr6:65779514-65779564	NH-A	brain:	n/a
48	chr6:65779514-65779564	HEEpiC	esophagus:	n/a
49	chr6:65779514-65779564	GM12891	blood:	n/a
50	chr6:65779514-65779564	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:65778187..65780499-chr6:65782117..65784614,2	K562	blood:
2	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
3	chr6:65644339..65646278-chr6:65650850..65653473,2	K562	blood:
4	chr6:65639435..65641072-chr6:65642848..65644357,2	MCF-7	breast:
5	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
6	chr6:65595975..65598086-chr6:65600070..65602994,2	K562	blood:
7	chr6:65761200..65763394-chr6:65766854..65768992,2	K562	blood:
8	chr6:65639435..65641072-chr6:65642848..65644357,2	MCF-7	breast:
9	chr6:65644339..65646278-chr6:65650850..65653473,2	K562	blood:
10	chr6:65695796..65698770-chr6:65700016..65702026,2	K562	blood:
11	chr6:65821770..65824951-chr6:65826871..65829970,3	K562	blood:
12	chr6:65781439..65783033-chr6:65783370..65784893,2	MCF-7	breast:
13	chr6:65821523..65823761-chr6:65825584..65828218,2	MCF-7	breast:
14	chr11:62312608..62314638-chr6:65744579..65746564,2	MCF-7	breast:
15	chr6:65781439..65783033-chr6:65783370..65784893,2	MCF-7	breast:
16	chr6:65821770..65824951-chr6:65826871..65829970,3	K562	blood:
17	chr6:65695796..65698770-chr6:65700016..65702026,2	K562	blood:
18	chr6:65821523..65823761-chr6:65825584..65828218,2	MCF-7	breast:
19	chr6:65761200..65763394-chr6:65766854..65768992,2	K562	blood:
20	chr6:65778187..65780499-chr6:65782117..65784614,2	K562	blood:
21	chr6:65595975..65598086-chr6:65600070..65602994,2	K562	blood:

Variant related genes	Relation type
ENSG00000256352	TF binding region
ENSG00000221312	TF binding region
ENSG00000256352	CpG island
ENSG00000221312	CpG island
ENSG00000124942	chromatin interactions
ENSG00000257058	chromatin interactions

Extended variants
information (count: 4393 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4393 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529677193	chr6:65588401-65588402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549430139	chr6:65588423-65588424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569420005	chr6:65588429-65588430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144444117	chr6:65588494-65588495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532125855	chr6:65588508-65588509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551996712	chr6:65588526-65588527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138946994	chr6:65588547-65588548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534954335	chr6:65588549-65588550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554647037	chr6:65588568-65588569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568416899	chr6:65588573-65588574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371609417	chr6:65588574-65588575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57000492	chr6:65588576-65588577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199791246	chr6:65588580-65588581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs398084985	chr6:65588583-65588584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs397955401	chr6:65588584-65588585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537459994	chr6:65588589-65588590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557451125	chr6:65588606-65588607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577419456	chr6:65588637-65588638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369980377	chr6:65588650-65588651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199550207	chr6:65588661-65588662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10485055	chr6:65588703-65588704	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs9363288	chr6:65588721-65588722	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539191177	chr6:65588802-65588803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573435209	chr6:65588809-65588810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367919045	chr6:65588818-65588819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187600801	chr6:65588828-65588829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562258042	chr6:65588840-65588841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192798977	chr6:65588874-65588875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9354184	chr6:65588875-65588876	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs575917174	chr6:65588917-65588918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528502496	chr6:65588934-65588935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543015524	chr6:65588948-65588949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563039190	chr6:65588949-65588950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182923068	chr6:65588964-65588965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552068870	chr6:65588974-65588975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559530457	chr6:65588978-65588979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9363289	chr6:65589020-65589021	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs13217880	chr6:65589054-65589055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568275232	chr6:65589056-65589057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537397748	chr6:65589074-65589075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146984663	chr6:65589085-65589086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570949017	chr6:65589094-65589095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539967427	chr6:65589095-65589096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75082237	chr6:65589118-65589119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376665473	chr6:65589135-65589136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573350596	chr6:65589151-65589152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188378261	chr6:65589153-65589154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555976866	chr6:65589178-65589179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7771761	chr6:65589229-65589230	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs9345563	chr6:65589237-65589238	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Epilepsy	20502679	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65588400-65589200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:65589200-65589800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:65589800-65590000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:65597400-65598200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr6:65598000-65598600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:65598200-65598400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr6:65598200-65600200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:65599200-65599800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:65599400-65599600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:65599600-65600000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:65599600-65600600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:65599800-65600600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr6:65600000-65600400	Enhancers	HUVEC	blood vessel
14	chr6:65600000-65600600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr6:65600200-65600600	Active TSS	Hela-S3	cervix
16	chr6:65600200-65601600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr6:65600200-65601800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:65600200-65603800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:65600400-65601000	Active TSS	NH-A	brain
20	chr6:65600400-65601600	Flanking Active TSS	HUVEC	blood vessel
21	chr6:65600600-65601200	Enhancers	Hela-S3	cervix
22	chr6:65600600-65601600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:65600600-65601600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:65600600-65601600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr6:65600600-65604200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:65600800-65601400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:65601000-65601400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:65601000-65601600	Enhancers	NH-A	brain
29	chr6:65601200-65601600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr6:65601200-65601600	Flanking Active TSS	Hela-S3	cervix
31	chr6:65601600-65602600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:65601600-65602600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr6:65601600-65602800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:65601600-65602800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr6:65601600-65602800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr6:65601600-65603000	Enhancers	HUVEC	blood vessel
37	chr6:65601800-65602200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr6:65602200-65603800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr6:65602600-65603200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr6:65602600-65603400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:65602800-65603200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr6:65602800-65603400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr6:65603000-65603200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:65612200-65613400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr6:65612600-65613400	Enhancers	Fetal Brain Female	brain
46	chr6:65613200-65613600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:65614000-65614600	Enhancers	HUVEC	blood vessel
48	chr6:65614200-65615400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr6:65614600-65615000	Flanking Active TSS	HUVEC	blood vessel
50	chr6:65615000-65615600	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links