Variant report

Variant	nsv1512
Chromosome Location	chr15:43616834-43661646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:959)
CpG islands
(count:1406)
Chromatin interactive
region (count:69)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43622452-43622973	K562	blood:	n/a	n/a
2	ARID3A	chr15:43622413-43623050	HepG2	liver:	n/a	n/a
3	ATF1	chr15:43622324-43623046	K562	blood:	n/a	n/a
4	ATF2	chr15:43622279-43623055	GM12878	blood:	n/a	n/a
5	BACH1	chr15:43622363-43623043	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr15:43621722-43621816	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr15:43622398-43622861	GM12878	blood:	n/a	n/a
8	BCL3	chr15:43622556-43623132	A549	lung:	n/a	chr15:43622795-43622804 chr15:43622825-43622834
9	BCLAF1	chr15:43622102-43623002	GM12878	blood:	n/a	chr15:43622795-43622804 chr15:43622825-43622834
10	BCLAF1	chr15:43622131-43623066	GM12878	blood:	n/a	chr15:43622795-43622804 chr15:43622825-43622834
11	BHLHE40	chr15:43622334-43623212	HepG2	liver:	n/a	n/a
12	BHLHE40	chr15:43621915-43622007	K562	blood:	n/a	n/a
13	BHLHE40	chr15:43622260-43623117	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:43622224-43623125	K562	blood:	n/a	n/a
15	BRCA1	chr15:43622325-43623390	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr15:43622061-43623223	K562	blood:	n/a	n/a
17	CBX3	chr15:43653379-43654014	HCT-116	colon:	n/a	n/a
18	CBX3	chr15:43653238-43653989	K562	blood:	n/a	n/a
19	CBX3	chr15:43653429-43653901	K562	blood:	n/a	n/a
20	CBX3	chr15:43622322-43622907	K562	blood:	n/a	n/a
21	CCNT2	chr15:43621909-43622840	K562	blood:	n/a	n/a
22	CEBPB	chr15:43622576-43623265	K562	blood:	n/a	n/a
23	CEBPB	chr15:43622400-43623240	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:43620669-43620880	K562	blood:	n/a	n/a
25	CEBPB	chr15:43622487-43623152	GM12878	blood:	n/a	n/a
26	CEBPB	chr15:43620651-43620887	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:43622331-43623176	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr15:43622550-43623130	K562	blood:	n/a	n/a
29	CEBPB	chr15:43622544-43623110	HepG2	liver:	n/a	n/a
30	CEBPB	chr15:43622116-43622152	HepG2	liver:	n/a	n/a
31	CEBPD	chr15:43622531-43623017	HepG2	liver:	n/a	n/a
32	CEBPD	chr15:43622163-43623135	K562	blood:	n/a	n/a
33	CHD1	chr15:43621926-43623067	GM12878	blood:	n/a	n/a
34	CHD2	chr15:43622129-43623112	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr15:43622342-43623073	K562	blood:	n/a	n/a
36	CHD2	chr15:43653549-43653751	K562	blood:	n/a	n/a
37	CHD2	chr15:43621982-43623085	GM12878	blood:	n/a	n/a
38	CHD2	chr15:43622135-43623108	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr15:43622157-43623130	HepG2	liver:	n/a	n/a
40	CREB1	chr15:43622620-43622954	A549	lung:	n/a	n/a
41	CREB1	chr15:43621899-43623263	HepG2	liver:	n/a	n/a
42	CREB1	chr15:43621793-43623204	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr15:43622313-43623049	A549	lung:	n/a	n/a
44	CREB1	chr15:43622023-43623130	GM12878	blood:	n/a	n/a
45	CREB1	chr15:43622251-43623137	K562	blood:	n/a	n/a
46	CREB1	chr15:43622344-43623075	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr15:43621724-43623112	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr15:43622312-43623186	HepG2	liver:	n/a	n/a
49	CTCF	chr15:43638700-43638850	GM12873	blood:	n/a	n/a
50	CTCF	chr15:43648616-43648831	HCT-116	colon:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43622721-43622771	A549	lung:	n/a
2	chr15:43626905-43626955	Caco-2	colon:	n/a
3	chr15:43622946-43622996	LNCaP	prostate:	n/a
4	chr15:43622721-43622771	A549	lung:	n/a
5	chr15:43626905-43626955	Caco-2	colon:	n/a
6	chr15:43622946-43622996	LNCaP	prostate:	n/a
7	chr15:43622732-43622782	MCF10A-Er-Src	breast:	n/a
8	chr15:43618947-43618997	HAEpiC	amniotic membrane:	n/a
9	chr15:43651467-43651517	GM12892	blood:	n/a
10	chr15:43622253-43622303	Jurkat	blood:	n/a
11	chr15:43623139-43623189	PrEC	prostate:	n/a
12	chr15:43621948-43621998	HMEC	breast:	n/a
13	chr15:43622253-43622303	Hela-S3	cervix:	n/a
14	chr15:43622253-43622303	HPAEpiC	pulmonary alveolar:	n/a
15	chr15:43626905-43626955	ECC-1	luminal epithelium:	n/a
16	chr15:43622840-43622890	K562	blood:	n/a
17	chr15:43622732-43622782	Hela-S3	cervix:	n/a
18	chr15:43658652-43658702	SK-N-SH_RA	brain:	n/a
19	chr15:43622652-43622702	HUVEC	blood vessel:	n/a
20	chr15:43651467-43651517	NHDF-neo	bronchial:	n/a
21	chr15:43622652-43622702	HMEC	breast:	n/a
22	chr15:43622253-43622303	GM12891	blood:	n/a
23	chr15:43651467-43651517	PrEC	prostate:	n/a
24	chr15:43622840-43622890	SK-N-SH_RA	brain:	n/a
25	chr15:43622808-43622858	ProgFib	skin:	n/a
26	chr15:43632501-43632551	LNCaP	prostate:	n/a
27	chr15:43641462-43641512	NB4	blood:	n/a
28	chr15:43623139-43623189	NT2-D1	testis:	n/a
29	chr15:43622721-43622771	HCPEpiC	choroid plexus:	n/a
30	chr15:43623282-43623332	HCPEpiC	choroid plexus:	n/a
31	chr15:43622721-43622771	U87	brain:	n/a
32	chr15:43623096-43623146	ProgFib	skin:	n/a
33	chr15:43641462-43641512	HEEpiC	esophagus:	n/a
34	chr15:43622978-43623028	H1-hESC	embryonic stem cell:	embryo
35	chr15:43645055-43645105	AG10803	skin:	n/a
36	chr15:43651467-43651517	ovcar-3	ovarian:	n/a
37	chr15:43622652-43622702	NH-A	brain:	n/a
38	chr15:43626905-43626955	H1-hESC	embryonic stem cell:	embryo
39	chr15:43622988-43623038	HL-60	blood:	n/a
40	chr15:43626905-43626955	AG09309	skin:	n/a
41	chr15:43622978-43623028	HEEpiC	esophagus:	n/a
42	chr15:43622946-43622996	GM06990	blood:	n/a
43	chr15:43623139-43623189	HUVEC	blood vessel:	n/a
44	chr15:43641462-43641512	HCT-116	colon:	n/a
45	chr15:43623139-43623189	GM12892	blood:	n/a
46	chr15:43622978-43623028	AG04449	skin:	fetal
47	chr15:43622253-43622303	AG04450	lung:	fetal
48	chr15:43622988-43623038	GM06990	blood:	n/a
49	chr15:43623282-43623332	HUVEC	blood vessel:	n/a
50	chr15:43651467-43651517	Hepatocyte	liver:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:43641400..43644347-chr15:43658323..43660227,2	K562	blood:
2	chr15:43478134..43480191-chr15:43618410..43620274,2	K562	blood:
3	chr15:43620486..43624109-chr15:43661175..43665421,4	K562	blood:
4	chr15:43624808..43626801-chr15:43642714..43644540,2	K562	blood:
5	chr15:43479061..43481710-chr15:43621878..43623729,2	K562	blood:
6	chr15:43620486..43624109-chr15:43661175..43665421,4	K562	blood:
7	chr15:43621804..43624747-chr15:43628079..43629850,3	MCF-7	breast:
8	chr15:43618581..43624264-chr15:43661265..43664929,7	MCF-7	breast:
9	chr15:43620805..43624764-chr15:43626235..43634573,14	K562	blood:
10	chr15:43646115..43650025-chr15:43654953..43659195,5	K562	blood:
11	chr15:43426164..43427738-chr15:43647862..43650071,2	K562	blood:
12	chr15:43660016..43662796-chr15:43702586..43705983,3	K562	blood:
13	chr15:43397435..43400079-chr15:43619938..43624138,3	K562	blood:
14	chr15:43607344..43608879-chr15:43617306..43618965,2	MCF-7	breast:
15	chr15:43621044..43624825-chr15:43626235..43637209,16	K562	blood:
16	chr15:43476610..43478211-chr15:43620895..43622509,2	K562	blood:
17	chr15:43622327..43623006-chr7:26240757..26241505,2	Hela-S3	cervix:
18	chr15:43621538..43624484-chr15:43650651..43653663,4	MCF-7	breast:
19	chr15:43656566..43658328-chr15:43666497..43669071,2	K562	blood:
20	chr15:43622512..43623300-chr3:14988494..14989255,2	Hela-S3	cervix:
21	chr15:43621078..43623590-chr15:43801793..43804270,2	MCF-7	breast:
22	chr15:43625690..43629602-chr15:43629922..43634519,5	K562	blood:
23	chr15:43646115..43650025-chr15:43654953..43659195,5	K562	blood:
24	chr15:43618584..43620563-chr15:43643035..43645762,2	K562	blood:
25	chr15:43621044..43624825-chr15:43626235..43637209,16	K562	blood:
26	chr15:43600831..43603445-chr15:43617687..43619322,2	K562	blood:
27	chr15:43621240..43623334-chr15:43630351..43632942,2	MCF-7	breast:
28	chr15:43618584..43620563-chr15:43643035..43645762,2	K562	blood:
29	chr15:43635174..43636743-chr15:43638248..43639911,2	K562	blood:
30	chr15:43621803..43624734-chr15:43667473..43669999,2	K562	blood:
31	chr15:43618581..43624264-chr15:43661265..43664929,7	MCF-7	breast:
32	chr15:43619535..43624096-chr15:43662038..43665421,4	K562	blood:
33	chr15:43620224..43622600-chr15:43663902..43665478,2	MCF-7	breast:
34	chr15:43586588..43588941-chr15:43618040..43620629,3	K562	blood:
35	chr15:43641400..43644347-chr15:43658323..43660227,2	K562	blood:
36	chr15:43624808..43626801-chr15:43642714..43644540,2	K562	blood:
37	chr15:43631165..43633410-chr15:43636087..43639224,3	K562	blood:
38	chr15:43620805..43624764-chr15:43626235..43634573,14	K562	blood:
39	chr15:43632397..43634657-chr15:43658728..43661211,2	K562	blood:
40	chr15:43512947..43514821-chr15:43621121..43624112,2	K562	blood:
41	chr15:43584770..43587744-chr15:43618210..43620882,2	MCF-7	breast:
42	chr15:43638723..43640590-chr15:43663770..43665773,2	K562	blood:
43	chr15:43622340..43623012-chr16:27214629..27215612,2	Hela-S3	cervix:
44	chr15:43621200..43623287-chr15:43640681..43643730,3	MCF-7	breast:
45	chr15:43661645..43664142-chr15:43669573..43672436,3	MCF-7	breast:
46	chr15:43586330..43589415-chr15:43618040..43621005,4	K562	blood:
47	chr15:43645456..43647561-chr15:43650775..43652983,2	K562	blood:
48	chr15:43500155..43503014-chr15:43621772..43625357,3	K562	blood:
49	chr15:43635174..43636743-chr15:43638248..43639911,2	K562	blood:
50	chr1:22109386..22110022-chr15:43622257..43623111,2	Hela-S3	cervix:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUBGCP4-2	chr15:43624098-43624581	NONHSAT042064
2	lnc-TUBGCP4-2	chr15:43623023-43623057	NONHSAT042064
3	lnc-LCMT2-1	chr15:43650376-43652236	NONHSAT042065

No data

Variant related genes	Relation type
LCMT2	TF binding region
ADAL	TF binding region
TUBGCP4	TF binding region
LCMT2	CpG island
ADAL	CpG island
TUBGCP4	CpG island
ENSG00000173812	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000137822	chromatin interactions
ENSG00000177463	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000261687	chromatin interactions
ENSG00000152348	chromatin interactions
ENSG00000166963	chromatin interactions
ENSG00000140265	chromatin interactions
ENSG00000225733	chromatin interactions
ENSG00000168803	chromatin interactions
ENSG00000166947	chromatin interactions
ENSG00000159459	chromatin interactions
ENSG00000168806	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000137842	chromatin interactions
ENSG00000197061	chromatin interactions
ENSG00000166946	chromatin interactions
ENSG00000155666	chromatin interactions
ENSG00000090686	chromatin interactions

Extended variants
information (count: 1672 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1672 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35295618	chr15:43616839-43616840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113062893	chr15:43616840-43616841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374513325	chr15:43616865-43616866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62706561	chr15:43616866-43616867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71111811	chr15:43616868-43616869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79262446	chr15:43616869-43616870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200953301	chr15:43616870-43616871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75384461	chr15:43616871-43616872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531650953	chr15:43616942-43616943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149177746	chr15:43616960-43616961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146506931	chr15:43616961-43616962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575440538	chr15:43616979-43616980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544077369	chr15:43616993-43616994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561099566	chr15:43617095-43617096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139075751	chr15:43617133-43617134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142965208	chr15:43617154-43617155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546463899	chr15:43617169-43617170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559352144	chr15:43617175-43617176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113117941	chr15:43617182-43617183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551502204	chr15:43617256-43617257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200451946	chr15:43617264-43617265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397801966	chr15:43617266-43617267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571404257	chr15:43617284-43617285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539478472	chr15:43617310-43617311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78605437	chr15:43617341-43617342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558118668	chr15:43617354-43617355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566638215	chr15:43617359-43617360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147120571	chr15:43617375-43617376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550908241	chr15:43617384-43617385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535644828	chr15:43617415-43617416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567818168	chr15:43617449-43617450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189940440	chr15:43617468-43617469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs956391	chr15:43617493-43617494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs182529718	chr15:43617587-43617588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538632723	chr15:43617599-43617600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375805192	chr15:43617684-43617685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186568734	chr15:43617743-43617744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116004697	chr15:43617759-43617760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573855093	chr15:43617779-43617780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189781774	chr15:43617807-43617808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566143726	chr15:43617823-43617824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574555176	chr15:43617845-43617846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544779657	chr15:43617925-43617926	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540171805	chr15:43618105-43618106	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs556628621	chr15:43618127-43618128	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs560006589	chr15:43618195-43618196	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs76276497	chr15:43618231-43618232	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs541815564	chr15:43618233-43618234	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs71111812	chr15:43618265-43618266	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs528512645	chr15:43618268-43618269	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2073 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43609000-43620200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr15:43611600-43620200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr15:43613000-43620600	Weak transcription	Right Atrium	heart
4	chr15:43613600-43620200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:43615000-43621000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr15:43615600-43617600	Weak transcription	Adipose Nuclei	Adipose
7	chr15:43615600-43620600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr15:43615800-43620600	Weak transcription	Brain Substantia Nigra	brain
9	chr15:43616400-43619600	Weak transcription	Primary B cells from cord blood	blood
10	chr15:43616400-43620600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr15:43616400-43620600	Weak transcription	HSMM	muscle
12	chr15:43616800-43620200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:43616800-43620400	Weak transcription	Fetal Intestine Large	intestine
14	chr15:43616800-43620600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr15:43616800-43620600	Weak transcription	Fetal Brain Male	brain
16	chr15:43617000-43620000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:43617000-43620000	Weak transcription	NHDF-Ad	bronchial
18	chr15:43617000-43620600	Weak transcription	Fetal Lung	lung
19	chr15:43617000-43621200	Weak transcription	Osteobl	bone
20	chr15:43617200-43619600	Weak transcription	Brain Germinal Matrix	brain
21	chr15:43617200-43620600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:43617200-43620800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:43617400-43620600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr15:43617600-43617800	Enhancers	Primary hematopoietic stem cells	blood
25	chr15:43617600-43617800	Enhancers	Fetal Muscle Leg	muscle
26	chr15:43617600-43617800	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr15:43617600-43618000	Enhancers	GM12878-XiMat	blood
28	chr15:43617600-43618600	Enhancers	Adipose Nuclei	Adipose
29	chr15:43617600-43620600	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr15:43617600-43620600	Weak transcription	A549	lung
31	chr15:43617800-43618000	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr15:43617800-43618000	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr15:43617800-43619600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr15:43617800-43620200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr15:43617800-43620400	Weak transcription	Fetal Muscle Leg	muscle
36	chr15:43617800-43620600	Weak transcription	NHLF	lung
37	chr15:43617800-43620800	Enhancers	Psoas Muscle	Psoas
38	chr15:43618000-43618200	Enhancers	Fetal Muscle Trunk	muscle
39	chr15:43618000-43618600	Enhancers	Left Ventricle	heart
40	chr15:43618000-43620400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr15:43618000-43620600	Weak transcription	Small Intestine	intestine
42	chr15:43618000-43620600	Weak transcription	GM12878-XiMat	blood
43	chr15:43618200-43619600	Weak transcription	Fetal Muscle Trunk	muscle
44	chr15:43618200-43620400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr15:43618200-43620600	Weak transcription	Gastric	stomach
46	chr15:43618200-43620600	Weak transcription	HMEC	breast
47	chr15:43618200-43620800	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr15:43618200-43621400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr15:43618400-43618600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr15:43618400-43618600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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