Variant report

Variant	nsv886355
Chromosome Location	chr6:93166766-93530757
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	chr6:93520606-93520837	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:93357446-93357691	HepG2	liver:	n/a	n/a
3	ATF2	chr6:93520527-93520984	GM12878	blood:	n/a	n/a
4	BACH1	chr6:93398300-93398367	K562	blood:	n/a	n/a
5	BACH1	chr6:93487556-93487616	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:93286975-93287516	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:93419834-93420037	GM12878	blood:	n/a	chr6:93419955-93419965
8	BATF	chr6:93419841-93420063	GM12878	blood:	n/a	chr6:93419955-93419965
9	BCL11A	chr6:93520665-93520856	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:93520535-93520895	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:93515069-93515071	GM12878	blood:	n/a	n/a
12	CCNT2	chr6:93411289-93411396	K562	blood:	n/a	n/a
13	CEBPB	chr6:93381227-93381482	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:93466672-93467045	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:93297134-93298301	Hela-S3	cervix:	n/a	chr6:93297656-93297669 chr6:93297656-93297667 chr6:93297656-93297667 chr6:93298095-93298108 chr6:93297745-93297756
16	CEBPB	chr6:93232345-93232664	K562	blood:	n/a	chr6:93232509-93232520
17	CEBPB	chr6:93217314-93217632	Hela-S3	cervix:	n/a	chr6:93217486-93217497
18	CEBPB	chr6:93232302-93232694	HepG2	liver:	n/a	chr6:93232509-93232520
19	CEBPB	chr6:93281889-93282163	HepG2	liver:	n/a	chr6:93282027-93282038 chr6:93281977-93281990 chr6:93282090-93282103
20	CEBPB	chr6:93232337-93232697	H1-hESC	embryonic stem cell:	n/a	chr6:93232509-93232520
21	CEBPB	chr6:93284930-93285135	Hela-S3	cervix:	n/a	chr6:93285008-93285021
22	CEBPB	chr6:93381259-93381429	K562	blood:	n/a	n/a
23	CEBPB	chr6:93247894-93248365	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr6:93246602-93246927	IMR90	lung:	n/a	chr6:93246754-93246765
25	CEBPB	chr6:93357127-93357843	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:93428416-93428674	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:93184022-93184315	HepG2	liver:	n/a	chr6:93184178-93184189
28	CEBPB	chr6:93381265-93381480	K562	blood:	n/a	n/a
29	CEBPB	chr6:93384032-93384320	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr6:93217317-93217677	IMR90	lung:	n/a	chr6:93217486-93217497
31	CEBPB	chr6:93275098-93275123	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:93466671-93467059	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:93232331-93232683	Hela-S3	cervix:	n/a	chr6:93232509-93232520
34	CEBPB	chr6:93248732-93249073	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr6:93246609-93246921	HepG2	liver:	n/a	chr6:93246754-93246765
36	CEBPB	chr6:93222527-93222535	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr6:93178794-93179008	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:93204857-93205358	Hela-S3	cervix:	n/a	chr6:93205016-93205025 chr6:93205014-93205025
39	CEBPB	chr6:93246596-93246869	A549	lung:	n/a	chr6:93246754-93246765
40	CEBPB	chr6:93208024-93208242	HepG2	liver:	n/a	chr6:93208166-93208179 chr6:93208166-93208177 chr6:93208168-93208177 chr6:93208167-93208178 chr6:93208166-93208177 chr6:93208168-93208177 chr6:93208168-93208177 chr6:93208166-93208179 chr6:93208168-93208177
41	CEBPB	chr6:93208080-93208182	H1-hESC	embryonic stem cell:	n/a	chr6:93208166-93208179 chr6:93208166-93208177 chr6:93208168-93208177 chr6:93208167-93208178 chr6:93208166-93208177 chr6:93208168-93208177 chr6:93208168-93208177 chr6:93208166-93208179 chr6:93208168-93208177
42	CEBPB	chr6:93217375-93217646	A549	lung:	n/a	chr6:93217486-93217497
43	CEBPB	chr6:93281911-93282210	IMR90	lung:	n/a	chr6:93282027-93282038 chr6:93281977-93281990 chr6:93282090-93282103
44	CEBPB	chr6:93425700-93426179	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:93416669-93417053	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:93217334-93217656	HepG2	liver:	n/a	chr6:93217486-93217497
47	CEBPB	chr6:93392816-93393116	MCF-7	breast:	n/a	chr6:93392896-93392909
48	CEBPB	chr6:93232196-93232704	IMR90	lung:	n/a	chr6:93232509-93232520
49	CEBPB	chr6:93524679-93524769	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr6:93357370-93357708	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:93354486-93354536	PFSK-1	brain:	n/a
2	chr6:93354486-93354536	PFSK-1	brain:	n/a
3	chr6:93433256-93433306	IMR90	lung:	fetal
4	chr6:93433256-93433306	AG10803	skin:	n/a
5	chr6:93354486-93354536	HepG2	liver:	n/a
6	chr6:93433256-93433306	BE2_C	brain:	n/a
7	chr6:93354486-93354536	AG04450	lung:	fetal
8	chr6:93354363-93354413	AG09309	skin:	n/a
9	chr6:93354290-93354340	Hela-S3	cervix:	n/a
10	chr6:93433536-93433586	NHDF-neo	bronchial:	n/a
11	chr6:93433536-93433586	ProgFib	skin:	n/a
12	chr6:93354363-93354413	U87	brain:	n/a
13	chr6:93433536-93433586	Hepatocyte	liver:	n/a
14	chr6:93433536-93433586	T-47D	breast:	n/a
15	chr6:93354290-93354340	SAEC	small airway:	n/a
16	chr6:93354290-93354340	AG09309	skin:	n/a
17	chr6:93354290-93354340	CMK	blood:	n/a
18	chr6:93354486-93354536	HNPCEpiC	eye:	n/a
19	chr6:93433256-93433306	HNPCEpiC	eye:	n/a
20	chr6:93433256-93433306	HCT-116	colon:	n/a
21	chr6:93354290-93354340	ovcar-3	ovarian:	n/a
22	chr6:93354363-93354413	HCT-116	colon:	n/a
23	chr6:93433256-93433306	GM12891	blood:	n/a
24	chr6:93354363-93354413	Hela-S3	cervix:	n/a
25	chr6:93354486-93354536	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:93433536-93433586	MCF-7	breast:	n/a
27	chr6:93433536-93433586	Caco-2	colon:	n/a
28	chr6:93354486-93354536	HEK293	kidney:	embryo
29	chr6:93354290-93354340	NHDF-neo	bronchial:	n/a
30	chr6:93433256-93433306	HCPEpiC	choroid plexus:	n/a
31	chr6:93354290-93354340	PrEC	prostate:	n/a
32	chr6:93354363-93354413	HEK293	kidney:	embryo
33	chr6:93433256-93433306	GM19239	blood:	n/a
34	chr6:93354290-93354340	HUVEC	blood vessel:	n/a
35	chr6:93354363-93354413	Jurkat	blood:	n/a
36	chr6:93354363-93354413	GM12891	blood:	n/a
37	chr6:93354290-93354340	HAEpiC	amniotic membrane:	n/a
38	chr6:93354363-93354413	ovcar-3	ovarian:	n/a
39	chr6:93433536-93433586	SK-N-MC	brain:	n/a
40	chr6:93433536-93433586	PANC-1	pancreas:	n/a
41	chr6:93354363-93354413	NHDF-neo	bronchial:	n/a
42	chr6:93433256-93433306	NH-A	brain:	n/a
43	chr6:93433536-93433586	GM06990	blood:	n/a
44	chr6:93433256-93433306	SAEC	small airway:	n/a
45	chr6:93433256-93433306	HCM	heart:	n/a
46	chr6:93433536-93433586	HCT-116	colon:	n/a
47	chr6:93354363-93354413	AG09319	gingival:	n/a
48	chr6:93433256-93433306	Caco-2	colon:	n/a
49	chr6:93354363-93354413	SAEC	small airway:	n/a
50	chr6:93433256-93433306	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:93198648..93200949-chr6:93203987..93205670,2	MCF-7	breast:
2	chr6:93198648..93200949-chr6:93203987..93205670,2	MCF-7	breast:
3	chr6:93385781..93388055-chr6:93400298..93402260,2	K562	blood:
4	chr6:93385781..93388055-chr6:93400298..93402260,2	K562	blood:
5	chr6:93224517..93226588-chr6:93230542..93232211,2	MCF-7	breast:
6	chr1:149856793..149857686-chr6:93467433..93468168,2	Hela-S3	cervix:
7	chr6:93363497..93365006-chr6:93368725..93371221,2	K562	blood:
8	chr6:93363497..93365006-chr6:93368725..93371221,2	K562	blood:
9	chr6:93420272..93423132-chr6:93542767..93544331,2	K562	blood:
10	chr6:93520687..93521206-chr6:93726686..93727450,3	MCF-7	breast:
11	chr6:93224517..93226588-chr6:93230542..93232211,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPHA7-2	chr6:93299496-93299804	XLOC_005783
2	lnc-EPHA7-2	chr6:93299040-93299050	XLOC_005783
3	lnc-MANEA-17	chr6:93500171-93500382	NONHSAT114014
4	lnc-MANEA-18	chr6:93326547-93326634	NONHSAT114009
5	lnc-MANEA-18	chr6:93336766-93336870	NONHSAT114009
6	lnc-EPHA7-6	chr6:93489442-93489526	NONHSAT114013
7	lnc-EPHA7-6	chr6:93489761-93490268	NONHSAT114013
8	lnc-MANEA-18	chr6:93346654-93346669	NONHSAT114009

Variant related genes	Relation type
ENSG00000265419	TF binding region
ENSG00000238412	TF binding region
ENSG00000220908	TF binding region
ENSG00000221455	TF binding region
ENSG00000265419	CpG island
ENSG00000238412	CpG island
ENSG00000220908	CpG island
ENSG00000221455	CpG island

Extended variants
information (count: 5815 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:5815 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12524154	chr6:93166766-93166767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564038503	chr6:93166820-93166821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1946406	chr6:93166870-93166871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs552420859	chr6:93166872-93166873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559332579	chr6:93166898-93166899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1365706	chr6:93166954-93166955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548323633	chr6:93166968-93166969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190210899	chr6:93167024-93167025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181137282	chr6:93167025-93167026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549686093	chr6:93167040-93167041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377471600	chr6:93167052-93167053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569802211	chr6:93167053-93167054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140329110	chr6:93167057-93167058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186246312	chr6:93167114-93167115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1863660	chr6:93167170-93167171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11964782	chr6:93167176-93167177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2875634	chr6:93167215-93167216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs74956244	chr6:93167216-93167217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560677809	chr6:93167221-93167222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534597692	chr6:93167265-93167266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1863659	chr6:93167380-93167381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190768054	chr6:93167434-93167435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574433489	chr6:93167439-93167440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145490646	chr6:93167505-93167506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563747188	chr6:93167526-93167527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71736087	chr6:93167537-93167538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112766149	chr6:93167553-93167554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370658807	chr6:93167556-93167557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577327946	chr6:93167557-93167558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113356616	chr6:93167571-93167572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536963912	chr6:93167582-93167583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559617675	chr6:93167589-93167590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73754488	chr6:93167621-93167622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548164099	chr6:93167624-93167625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184053838	chr6:93167743-93167744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140508368	chr6:93167748-93167749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2555762	chr6:93167753-93167754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs188603973	chr6:93167859-93167860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371144779	chr6:93167901-93167902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567151974	chr6:93167906-93167907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376835863	chr6:93168008-93168009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569758369	chr6:93168021-93168022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538789731	chr6:93168046-93168047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146234368	chr6:93168054-93168055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371446823	chr6:93168056-93168057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201535081	chr6:93168068-93168069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201862520	chr6:93168069-93168070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199734347	chr6:93168070-93168071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144440675	chr6:93168071-93168072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370951141	chr6:93168072-93168073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adrenocortical carcinoma	18281524	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Neuropathy	19664229	CNVD
Neurodevelopmental disorder	22521361	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:93165200-93170200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr6:93169400-93169800	Enhancers	HUVEC	blood vessel
3	chr6:93169400-93170200	Enhancers	HSMMtube	muscle
4	chr6:93169400-93171200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:93170000-93170400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:93170000-93170800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:93170200-93171000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:93170200-93171000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:93170200-93171200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:93173000-93173400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:93182200-93182600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:93182200-93182800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:93182400-93182800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr6:93182400-93182800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr6:93182400-93182800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:93182800-93183600	Enhancers	HUVEC	blood vessel
17	chr6:93189400-93190200	Enhancers	HUVEC	blood vessel
18	chr6:93189600-93190000	Enhancers	Fetal Heart	heart
19	chr6:93190000-93191400	Weak transcription	Fetal Heart	heart
20	chr6:93191400-93192000	Enhancers	Fetal Heart	heart
21	chr6:93192000-93198000	Weak transcription	Fetal Heart	heart
22	chr6:93198000-93199000	Enhancers	Fetal Heart	heart
23	chr6:93204200-93205000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr6:93204400-93205200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr6:93205000-93205200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:93205000-93206000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:93205200-93206200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:93205200-93206200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:93206200-93206400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr6:93206200-93206600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr6:93206200-93206600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:93206200-93206600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:93206200-93206600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr6:93206200-93206600	Enhancers	Ovary	ovary
35	chr6:93206200-93206800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:93206800-93207800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr6:93207800-93208200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:93230600-93232400	Enhancers	HUVEC	blood vessel
39	chr6:93231600-93232000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:93236200-93236600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:93236600-93236800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:93244000-93244600	Enhancers	Fetal Heart	heart
43	chr6:93244600-93248000	Weak transcription	Fetal Heart	heart
44	chr6:93245400-93246000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:93247400-93250600	Enhancers	HUVEC	blood vessel
46	chr6:93247800-93248400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:93247800-93248600	Enhancers	Hela-S3	cervix
48	chr6:93247800-93248600	Enhancers	NH-A	brain
49	chr6:93247800-93248800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:93248000-93248400	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links