Variant report

Variant	esv35102
Chromosome Location	chr6:162827464-163057269
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	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
3	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
4	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
5	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
6	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
7	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
8	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
9	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
13	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
14	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
16	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
17	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
21	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
23	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
24	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
25	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
26	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
27	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
28	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
29	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
30	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
31	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
32	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
33	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
34	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
35	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
37	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
39	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
40	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
41	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
42	CEBPD	chr6:162857313-162857505	HepG2	liver:	n/a	n/a
43	CHD2	chr6:162863812-162864012	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr6:162977640-162977790	NHEK	skin:	n/a	n/a
45	CTCF	chr6:162863693-162864122	HepG2	liver:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932
46	CTCF	chr6:162863860-162864010	HMF	breast:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932
47	CTCF	chr6:162838260-162838410	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:162863840-162863990	HPF	lung:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932
49	CTCF	chr6:162863760-162863910	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:162863820-162863970	HepG2	liver:	n/a	chr6:162863909-162863927 chr6:162863912-162863921 chr6:162863911-162863932

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162865171-162865221	HAEpiC	amniotic membrane:	n/a
2	chr6:162865171-162865221	HAEpiC	amniotic membrane:	n/a
3	chr6:162964378-162964428	IMR90	lung:	fetal
4	chr6:162831837-162831887	AG04450	lung:	fetal
5	chr6:162865258-162865308	Hela-S3	cervix:	n/a
6	chr6:162964378-162964428	BE2_C	brain:	n/a
7	chr6:162831837-162831887	GM12892	blood:	n/a
8	chr6:163024624-163024674	HMEC	breast:	n/a
9	chr6:162865258-162865308	K562	blood:	n/a
10	chr6:162864586-162864636	NT2-D1	testis:	n/a
11	chr6:163024624-163024674	ECC-1	luminal epithelium:	n/a
12	chr6:162863505-162863555	U87	brain:	n/a
13	chr6:162865258-162865308	GM12892	blood:	n/a
14	chr6:162831837-162831887	BE2_C	brain:	n/a
15	chr6:162865171-162865221	GM06990	blood:	n/a
16	chr6:163024624-163024674	U87	brain:	n/a
17	chr6:162863505-162863555	LNCaP	prostate:	n/a
18	chr6:162865258-162865308	Caco-2	colon:	n/a
19	chr6:162863505-162863555	SAEC	small airway:	n/a
20	chr6:163024624-163024674	PANC-1	pancreas:	n/a
21	chr6:162864586-162864636	NH-A	brain:	n/a
22	chr6:162863505-162863555	AG10803	skin:	n/a
23	chr6:162964378-162964428	H1-hESC	embryonic stem cell:	embryo
24	chr6:162864586-162864636	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:162964378-162964428	RPTEC	kidney:	n/a
26	chr6:162831837-162831887	NH-A	brain:	n/a
27	chr6:162865258-162865308	AG09309	skin:	n/a
28	chr6:162865258-162865308	HEK293	kidney:	embryo
29	chr6:162865171-162865221	AG04450	lung:	fetal
30	chr6:162865258-162865308	HCF	heart:	n/a
31	chr6:163024624-163024674	Caco-2	colon:	n/a
32	chr6:162863505-162863555	HEK293	kidney:	embryo
33	chr6:162865171-162865221	AG09309	skin:	n/a
34	chr6:162863505-162863555	CMK	blood:	n/a
35	chr6:162964378-162964428	Hepatocyte	liver:	n/a
36	chr6:162831837-162831887	MCF-7	breast:	n/a
37	chr6:162831837-162831887	AoSMC	blood vessel:	n/a
38	chr6:163024624-163024674	SK-N-MC	brain:	n/a
39	chr6:162864586-162864636	SKMC	muscle:	n/a
40	chr6:162964378-162964428	HCF	heart:	n/a
41	chr6:163024624-163024674	BJ	skin:	n/a
42	chr6:162831837-162831887	HRPEpiC	eye:	n/a
43	chr6:163024624-163024674	H1-hESC	embryonic stem cell:	embryo
44	chr6:162865171-162865221	HL-60	blood:	n/a
45	chr6:162865258-162865308	HMEC	breast:	n/a
46	chr6:163024624-163024674	HCPEpiC	choroid plexus:	n/a
47	chr6:162964378-162964428	PrEC	prostate:	n/a
48	chr6:163024624-163024674	GM19239	blood:	n/a
49	chr6:163024624-163024674	HepG2	liver:	n/a
50	chr6:162865258-162865308	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
2	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
3	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
4	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
5	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
6	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
7	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
8	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
9	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 9840 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:9840 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6904788	chr6:162827464-162827465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558434199	chr6:162827474-162827475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578178755	chr6:162827492-162827493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139646818	chr6:162827496-162827497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552975026	chr6:162827498-162827499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577726554	chr6:162827506-162827507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545083643	chr6:162827525-162827526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563251403	chr6:162827565-162827566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573814465	chr6:162827570-162827571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574316736	chr6:162827578-162827579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144290645	chr6:162827599-162827600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190841608	chr6:162827657-162827658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6924255	chr6:162827677-162827678	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551278058	chr6:162827703-162827704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146726421	chr6:162827733-162827734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530697002	chr6:162827735-162827736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140319636	chr6:162827748-162827749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368077691	chr6:162827783-162827784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371529589	chr6:162827789-162827790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535431766	chr6:162827808-162827809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549066935	chr6:162827815-162827816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142706445	chr6:162827854-162827855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535259266	chr6:162827864-162827865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537503120	chr6:162827871-162827872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376623271	chr6:162827942-162827943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542846334	chr6:162827961-162827962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183129061	chr6:162827966-162827967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557652616	chr6:162827994-162827995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573699357	chr6:162828011-162828012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151002403	chr6:162828064-162828065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75485706	chr6:162828082-162828083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572849671	chr6:162828100-162828101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114968775	chr6:162828117-162828118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528413285	chr6:162828121-162828122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564918744	chr6:162828147-162828148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369351486	chr6:162828156-162828157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4709606	chr6:162828192-162828193	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs550485393	chr6:162828223-162828224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560800571	chr6:162828250-162828251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138646878	chr6:162828267-162828268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548954327	chr6:162828269-162828270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566209252	chr6:162828335-162828336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528556387	chr6:162828375-162828376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545115744	chr6:162828386-162828387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60653626	chr6:162828416-162828417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186659475	chr6:162828438-162828439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546375564	chr6:162828474-162828475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376015214	chr6:162828488-162828489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191115247	chr6:162828492-162828493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77742184	chr6:162828526-162828527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162823400-162830800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:162827200-162827600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr6:162827600-162828000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:162828000-162833400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:162828200-162828400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:162828200-162828800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr6:162828200-162829000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:162828200-162830800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:162828400-162828600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:162828400-162829000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:162828400-162831200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:162828400-162831400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:162828600-162829200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:162828600-162830000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:162828800-162830600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr6:162829000-162829400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:162829000-162829400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:162829200-162833400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:162829200-162833600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:162829400-162829600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:162829400-162829600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr6:162829400-162830800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:162829600-162830800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:162829600-162831200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr6:162829800-162831000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:162830000-162830600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr6:162830200-162830800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:162830200-162832800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:162830400-162830600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:162830400-162831600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:162830600-162830800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr6:162830600-162831600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:162830600-162833200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:162830800-162831000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr6:162830800-162831000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:162830800-162831200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr6:162830800-162831200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr6:162830800-162831200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr6:162830800-162831800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:162830800-162832000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:162831000-162831600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:162831000-162831600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr6:162831000-162831800	Enhancers	Brain Germinal Matrix	brain
44	chr6:162831000-162832000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr6:162831200-162831400	Active TSS	H1 Cell Line	embryonic stem cell
46	chr6:162831200-162831600	Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr6:162831200-162831600	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr6:162831200-162831800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr6:162831200-162832000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr6:162831200-162832000	Enhancers	Brain Hippocampus Middle	brain

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