Variant report

Variant	nsv1020080
Chromosome Location	chr6:162745568-163039183
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	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
4	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
5	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
6	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
7	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
8	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
9	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
10	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
11	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
14	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
15	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
16	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
17	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
20	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
21	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
22	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
23	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
24	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
25	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
26	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
27	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
28	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
30	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
31	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
32	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
33	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
35	CEBPB	chr6:162766332-162766577	H1-hESC	embryonic stem cell:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
36	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
37	CEBPB	chr6:162766335-162766614	A549	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
38	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
40	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:162766353-162766628	IMR90	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
42	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
43	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
44	CEBPB	chr6:162766327-162766640	HepG2	liver:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
45	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
46	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
48	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
49	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
50	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162964378-162964428	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:162863505-162863555	AG04450	lung:	fetal
3	chr6:162865171-162865221	HRCEpiC	kidney:	n/a
4	chr6:162864586-162864636	GM12892	blood:	n/a
5	chr6:162865258-162865308	AG09319	gingival:	n/a
6	chr6:162865171-162865221	HRPEpiC	eye:	n/a
7	chr6:163024624-163024674	GM12891	blood:	n/a
8	chr6:162964378-162964428	BE2_C	brain:	n/a
9	chr6:162863505-162863555	T-47D	breast:	n/a
10	chr6:162964378-162964428	HepG2	liver:	n/a
11	chr6:162863505-162863555	NHDF-neo	bronchial:	n/a
12	chr6:162964378-162964428	ovcar-3	ovarian:	n/a
13	chr6:162865258-162865308	SAEC	small airway:	n/a
14	chr6:163024624-163024674	HEEpiC	esophagus:	n/a
15	chr6:163024624-163024674	Jurkat	blood:	n/a
16	chr6:163024624-163024674	H1-hESC	embryonic stem cell:	embryo
17	chr6:162964378-162964428	HCM	heart:	n/a
18	chr6:162964378-162964428	AoSMC	blood vessel:	n/a
19	chr6:162964378-162964428	GM12878	blood:	n/a
20	chr6:162831837-162831887	SK-N-SH	brain:	n/a
21	chr6:163024624-163024674	K562	blood:	n/a
22	chr6:162964378-162964428	SK-N-SH_RA	brain:	n/a
23	chr6:163024624-163024674	GM19239	blood:	n/a
24	chr6:162865258-162865308	HAEpiC	amniotic membrane:	n/a
25	chr6:162865171-162865221	AG04449	skin:	fetal
26	chr6:162831837-162831887	HEK293	kidney:	embryo
27	chr6:162831837-162831887	SAEC	small airway:	n/a
28	chr6:162865171-162865221	SKMC	muscle:	n/a
29	chr6:162864586-162864636	HMEC	breast:	n/a
30	chr6:162864586-162864636	HCPEpiC	choroid plexus:	n/a
31	chr6:162864586-162864636	SK-N-SH_RA	brain:	n/a
32	chr6:162964378-162964428	H1-hESC	embryonic stem cell:	embryo
33	chr6:162863505-162863555	ECC-1	luminal epithelium:	n/a
34	chr6:162865171-162865221	HCM	heart:	n/a
35	chr6:162863505-162863555	HCT-116	colon:	n/a
36	chr6:163024624-163024674	HUVEC	blood vessel:	n/a
37	chr6:163024624-163024674	SAEC	small airway:	n/a
38	chr6:162831837-162831887	HUVEC	blood vessel:	n/a
39	chr6:162864586-162864636	T-47D	breast:	n/a
40	chr6:162964378-162964428	NB4	blood:	n/a
41	chr6:162964378-162964428	SKMC	muscle:	n/a
42	chr6:162863505-162863555	CMK	blood:	n/a
43	chr6:162964378-162964428	AG10803	skin:	n/a
44	chr6:162864586-162864636	Jurkat	blood:	n/a
45	chr6:162863505-162863555	A549	lung:	n/a
46	chr6:162865171-162865221	PFSK-1	brain:	n/a
47	chr6:162865171-162865221	NT2-D1	testis:	n/a
48	chr6:162863505-162863555	HepG2	liver:	n/a
49	chr6:162863505-162863555	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:162865171-162865221	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
2	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
3	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
4	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
5	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
6	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
7	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
8	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
9	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
10	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
11	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
12	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
13	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
14	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
15	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
16	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
17	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: 12370 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:12370 , 50 per page) page: 1 2 3 4 5 6 7 ... 248

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190093626	chr6:162745584-162745585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181629495	chr6:162745601-162745602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572489720	chr6:162745605-162745606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548134680	chr6:162745619-162745620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185803737	chr6:162745630-162745631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558282239	chr6:162745732-162745733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77369688	chr6:162745747-162745748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533844748	chr6:162745763-162745764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578252018	chr6:162745814-162745815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544092960	chr6:162745817-162745818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563292856	chr6:162745952-162745953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533874137	chr6:162745959-162745960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199663076	chr6:162745962-162745963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547629839	chr6:162745964-162745965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146140115	chr6:162745967-162745968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529950809	chr6:162745970-162745971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372973395	chr6:162745973-162745974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71544929	chr6:162745978-162745979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201217446	chr6:162745979-162745980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558489290	chr6:162745992-162745993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114113362	chr6:162746025-162746026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551850223	chr6:162746032-162746033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559230168	chr6:162746048-162746049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190357889	chr6:162746081-162746082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144921041	chr6:162746105-162746106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564705099	chr6:162746145-162746146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs151251252	chr6:162746171-162746172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71814594	chr6:162746172-162746173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75305414	chr6:162746173-162746174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74552382	chr6:162746174-162746175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537878964	chr6:162746256-162746257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4708953	chr6:162746266-162746267	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs141296466	chr6:162746330-162746331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550491676	chr6:162746349-162746350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574880182	chr6:162746350-162746351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6930880	chr6:162746359-162746360	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs372527621	chr6:162746375-162746376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554079098	chr6:162746391-162746392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183962615	chr6:162746430-162746431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549352285	chr6:162746469-162746470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566040994	chr6:162746515-162746516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572664495	chr6:162746526-162746527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117784585	chr6:162746580-162746581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558081673	chr6:162746595-162746596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564797423	chr6:162746606-162746607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578196109	chr6:162746608-162746609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537618994	chr6:162746628-162746629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12193134	chr6:162746641-162746642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544266191	chr6:162746666-162746667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574378603	chr6:162746679-162746680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162728000-162765600	Weak transcription	Pancreas	Pancrea
2	chr6:162745800-162746600	Enhancers	Fetal Brain Male	brain
3	chr6:162746000-162746800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:162746200-162746600	Enhancers	Fetal Lung	lung
5	chr6:162746400-162746800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:162746600-162747400	Weak transcription	Fetal Brain Male	brain
7	chr6:162747400-162747600	Enhancers	Fetal Brain Male	brain
8	chr6:162747400-162749800	Weak transcription	Ovary	ovary
9	chr6:162749600-162753000	Weak transcription	Aorta	Aorta
10	chr6:162749800-162750000	Strong transcription	Ovary	ovary
11	chr6:162750000-162753800	Weak transcription	Ovary	ovary
12	chr6:162753200-162753600	Enhancers	Adipose Nuclei	Adipose
13	chr6:162753600-162761000	Weak transcription	Adipose Nuclei	Adipose
14	chr6:162755000-162766200	Weak transcription	Ovary	ovary
15	chr6:162757800-162758000	Enhancers	Gastric	stomach
16	chr6:162757800-162758800	Enhancers	Fetal Heart	heart
17	chr6:162758600-162758800	Enhancers	Gastric	stomach
18	chr6:162761400-162761600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:162761600-162766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:162762600-162763000	Weak transcription	Adipose Nuclei	Adipose
21	chr6:162763400-162763800	Enhancers	Fetal Lung	lung
22	chr6:162763600-162764200	Enhancers	Stomach Mucosa	stomach
23	chr6:162763800-162765200	Weak transcription	Fetal Lung	lung
24	chr6:162764000-162764600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:162764400-162764800	Enhancers	Brain Cingulate Gyrus	brain
26	chr6:162764400-162765400	Active TSS	Adipose Nuclei	Adipose
27	chr6:162764400-162766200	Enhancers	Fetal Muscle Leg	muscle
28	chr6:162764400-162766400	Enhancers	NHDF-Ad	bronchial
29	chr6:162764400-162766800	Enhancers	Brain Hippocampus Middle	brain
30	chr6:162764400-162767200	Enhancers	HMEC	breast
31	chr6:162764400-162767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:162764400-162767600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:162764600-162765400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:162764600-162766400	Enhancers	Fetal Brain Male	brain
35	chr6:162764600-162767000	Enhancers	Fetal Heart	heart
36	chr6:162764800-162765400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:162764800-162766200	Weak transcription	Brain Cingulate Gyrus	brain
38	chr6:162765000-162765400	Enhancers	HSMM	muscle
39	chr6:162765000-162765600	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr6:162765000-162765800	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr6:162765000-162766200	Enhancers	Brain Substantia Nigra	brain
42	chr6:162765000-162766400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:162765000-162766400	Enhancers	Brain Angular Gyrus	brain
44	chr6:162765000-162766400	Enhancers	Right Atrium	heart
45	chr6:162765000-162766800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr6:162765000-162767200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:162765000-162767200	Enhancers	NHEK	skin
48	chr6:162765200-162765600	Enhancers	Fetal Lung	lung
49	chr6:162765200-162766200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:162765200-162767000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links