Variant report

Variant	nsv1023779
Chromosome Location	chr6:162780855-163042505
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	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
4	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
5	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
6	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
7	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
8	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
9	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
10	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
11	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
12	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
13	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
14	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
15	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
17	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
19	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
20	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
21	CEBPB	chr6:162784733-162785018	K562	blood:	n/a	n/a
22	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
23	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
24	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
25	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
27	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
28	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
29	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
30	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
32	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
33	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
34	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
35	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
36	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
37	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
38	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
39	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
41	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
42	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
43	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
44	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
45	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
47	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
48	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
50	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162864586-162864636	HRPEpiC	eye:	n/a
2	chr6:162831837-162831887	CMK	blood:	n/a
3	chr6:162831837-162831887	GM12878	blood:	n/a
4	chr6:162863505-162863555	NHBE	bronchial:	n/a
5	chr6:162865258-162865308	HCT-116	colon:	n/a
6	chr6:162864586-162864636	GM06990	blood:	n/a
7	chr6:162964378-162964428	HepG2	liver:	n/a
8	chr6:162863505-162863555	NHDF-neo	bronchial:	n/a
9	chr6:163024624-163024674	AG10803	skin:	n/a
10	chr6:162863505-162863555	PrEC	prostate:	n/a
11	chr6:162964378-162964428	AG09319	gingival:	n/a
12	chr6:163024624-163024674	Jurkat	blood:	n/a
13	chr6:162865258-162865308	HRCEpiC	kidney:	n/a
14	chr6:162865171-162865221	AG09309	skin:	n/a
15	chr6:162864586-162864636	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:162864586-162864636	GM12891	blood:	n/a
17	chr6:162865171-162865221	HIPEpiC	eye:	n/a
18	chr6:162865171-162865221	HRCEpiC	kidney:	n/a
19	chr6:162863505-162863555	HRCEpiC	kidney:	n/a
20	chr6:162865171-162865221	SK-N-SH	brain:	n/a
21	chr6:162864586-162864636	MCF10A-Er-Src	breast:	n/a
22	chr6:162964378-162964428	AG09309	skin:	n/a
23	chr6:162863505-162863555	HCPEpiC	choroid plexus:	n/a
24	chr6:162863505-162863555	SAEC	small airway:	n/a
25	chr6:162964378-162964428	LNCaP	prostate:	n/a
26	chr6:163024624-163024674	BJ	skin:	n/a
27	chr6:162863505-162863555	HRE	kidney:	n/a
28	chr6:162831837-162831887	PANC-1	pancreas:	n/a
29	chr6:162831837-162831887	AG04450	lung:	fetal
30	chr6:162863505-162863555	SK-N-SH_RA	brain:	n/a
31	chr6:162865171-162865221	T-47D	breast:	n/a
32	chr6:162831837-162831887	ECC-1	luminal epithelium:	n/a
33	chr6:162865258-162865308	HCM	heart:	n/a
34	chr6:162831837-162831887	ProgFib	skin:	n/a
35	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:162865171-162865221	IMR90	lung:	fetal
37	chr6:162863505-162863555	U87	brain:	n/a
38	chr6:162865258-162865308	AoSMC	blood vessel:	n/a
39	chr6:163024624-163024674	HRPEpiC	eye:	n/a
40	chr6:162864586-162864636	IMR90	lung:	fetal
41	chr6:163024624-163024674	Caco-2	colon:	n/a
42	chr6:162865258-162865308	SKMC	muscle:	n/a
43	chr6:163024624-163024674	PANC-1	pancreas:	n/a
44	chr6:162865258-162865308	H1-hESC	embryonic stem cell:	embryo
45	chr6:162865171-162865221	AG04449	skin:	fetal
46	chr6:163024624-163024674	GM19239	blood:	n/a
47	chr6:162831837-162831887	SKMC	muscle:	n/a
48	chr6:162865171-162865221	Hepatocyte	liver:	n/a
49	chr6:163024624-163024674	CMK	blood:	n/a
50	chr6:162865171-162865221	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
2	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
3	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
4	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
5	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
6	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
7	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
8	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
9	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
10	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
11	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
12	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
13	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
14	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:

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

Extended variants
information (count: 11264 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:11264 , 50 per page) page: 1 2 3 4 5 6 7 ... 226

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183363119	chr6:162780870-162780871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541505963	chr6:162780946-162780947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79028032	chr6:162780995-162780996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs578077796	chr6:162781017-162781018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78703859	chr6:162781018-162781019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187216863	chr6:162781046-162781047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528892194	chr6:162781086-162781087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190937476	chr6:162781099-162781100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79808870	chr6:162781111-162781112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62430700	chr6:162781126-162781127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551149114	chr6:162781146-162781147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76647326	chr6:162781153-162781154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536889872	chr6:162781202-162781203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150200375	chr6:162781209-162781210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs16893736	chr6:162781257-162781258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550890952	chr6:162781258-162781259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138720042	chr6:162781282-162781283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182838223	chr6:162781307-162781308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547153827	chr6:162781382-162781383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369349537	chr6:162781400-162781401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149388145	chr6:162781404-162781405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566040456	chr6:162781429-162781430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535129262	chr6:162781471-162781472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147472790	chr6:162781489-162781490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188089857	chr6:162781522-162781523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191715288	chr6:162781529-162781530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142791255	chr6:162781546-162781547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147435927	chr6:162781547-162781548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574014145	chr6:162781551-162781552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376369113	chr6:162781562-162781563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578014574	chr6:162781595-162781596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542876724	chr6:162781603-162781604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569809130	chr6:162781618-162781619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558930291	chr6:162781637-162781638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572456381	chr6:162781640-162781641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545465263	chr6:162781670-162781671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs16893737	chr6:162781681-162781682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148491306	chr6:162781754-162781755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563669571	chr6:162781783-162781784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530766970	chr6:162781785-162781786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs16893740	chr6:162781811-162781812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs142672126	chr6:162781836-162781837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548482079	chr6:162781900-162781901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182539919	chr6:162781916-162781917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150944299	chr6:162781932-162781933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139440270	chr6:162781945-162781946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534702237	chr6:162782025-162782026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61416814	chr6:162782074-162782075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549166894	chr6:162782082-162782083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377713542	chr6:162782111-162782112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Schizophrenia	20967226	CNVD
Attention deficit hyperactivity disorder	19546859	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:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162780000-162785000	Weak transcription	Left Ventricle	heart
2	chr6:162780000-162789000	Weak transcription	Ovary	ovary
3	chr6:162780000-162789400	Weak transcription	Fetal Heart	heart
4	chr6:162782200-162782600	Enhancers	Aorta	Aorta
5	chr6:162782200-162782600	Enhancers	Right Ventricle	heart
6	chr6:162784200-162785800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr6:162784600-162785400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:162784800-162785200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:162784800-162785200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:162784800-162785200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr6:162784800-162785400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:162784800-162785400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr6:162784800-162785800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:162785000-162785400	Enhancers	Left Ventricle	heart
15	chr6:162785000-162785600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:162785200-162786800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:162785400-162785600	Weak transcription	Left Ventricle	heart
18	chr6:162785400-162789000	Weak transcription	Right Atrium	heart
19	chr6:162785400-162793000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:162785600-162785800	Enhancers	Left Ventricle	heart
21	chr6:162785800-162806600	Weak transcription	Left Ventricle	heart
22	chr6:162789000-162789800	Strong transcription	Ovary	ovary
23	chr6:162789000-162789800	Enhancers	Right Atrium	heart
24	chr6:162789000-162790200	Enhancers	Right Ventricle	heart
25	chr6:162789000-162791000	Enhancers	Aorta	Aorta
26	chr6:162789400-162790200	Enhancers	Fetal Heart	heart
27	chr6:162789800-162792600	Weak transcription	Ovary	ovary
28	chr6:162789800-162792800	Weak transcription	Right Atrium	heart
29	chr6:162790200-162790800	Weak transcription	Right Ventricle	heart
30	chr6:162790800-162791000	Enhancers	Right Ventricle	heart
31	chr6:162791000-162793000	Weak transcription	Psoas Muscle	Psoas
32	chr6:162792000-162793600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr6:162792200-162792600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:162792200-162793800	Enhancers	Pancreas	Pancrea
35	chr6:162792600-162798000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:162792800-162793200	Enhancers	Right Atrium	heart
37	chr6:162792800-162793600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr6:162792800-162795400	Enhancers	Liver	Liver
39	chr6:162793000-162793600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:162793000-162793600	Enhancers	Adipose Nuclei	Adipose
41	chr6:162793400-162795200	Enhancers	HepG2	liver
42	chr6:162793600-162796800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr6:162793800-162798600	Weak transcription	Pancreas	Pancrea
44	chr6:162794400-162795200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr6:162795400-162798600	Weak transcription	Liver	Liver
46	chr6:162796800-162799000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:162797600-162798000	Active TSS	HSMM	muscle
48	chr6:162798000-162798400	Enhancers	Aorta	Aorta
49	chr6:162798000-162800600	Weak transcription	HSMM	muscle
50	chr6:162798000-162802200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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