Variant report

Variant	nsv510667
Chromosome Location	chr15:76653359-76708310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:123)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:76702660-76702679	K562	blood:	n/a	n/a
2	CEBPB	chr15:76678493-76678990	MCF-7	breast:	n/a	n/a
3	CEBPB	chr15:76662838-76663129	HepG2	liver:	n/a	chr15:76662979-76662990
4	CEBPB	chr15:76693651-76693876	K562	blood:	n/a	n/a
5	CEBPB	chr15:76702091-76702291	IMR90	lung:	n/a	chr15:76702198-76702209
6	CEBPB	chr15:76662934-76663134	K562	blood:	n/a	chr15:76662979-76662990
7	CEBPB	chr15:76662856-76663116	A549	lung:	n/a	chr15:76662979-76662990
8	CEBPB	chr15:76662968-76663047	Hela-S3	cervix:	n/a	chr15:76662979-76662990
9	CEBPB	chr15:76693557-76694015	MCF-7	breast:	n/a	n/a
10	CEBPB	chr15:76693587-76693973	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr15:76662910-76663148	IMR90	lung:	n/a	chr15:76662979-76662990
12	CEBPB	chr15:76693596-76693959	IMR90	lung:	n/a	n/a
13	CEBPB	chr15:76693458-76694018	MCF-7	breast:	n/a	n/a
14	CEBPB	chr15:76702108-76702227	K562	blood:	n/a	chr15:76702198-76702209
15	CEBPB	chr15:76678585-76678838	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:76702054-76702304	A549	lung:	n/a	chr15:76702198-76702209
17	CEBPB	chr15:76702033-76702336	HepG2	liver:	n/a	chr15:76702198-76702209
18	CEBPB	chr15:76702131-76702227	Hela-S3	cervix:	n/a	chr15:76702198-76702209
19	CEBPB	chr15:76702139-76702250	H1-hESC	embryonic stem cell:	n/a	chr15:76702198-76702209
20	CHD2	chr15:76668708-76668724	HepG2	liver:	n/a	n/a
21	CTCF	chr15:76662173-76662260	MCF-7	breast:	n/a	n/a
22	CTCF	chr15:76662213-76662284	GM19239	blood:	n/a	n/a
23	CTCF	chr15:76662189-76662257	GM12892	blood:	n/a	n/a
24	CTCF	chr15:76662182-76662252	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:76656860-76657010	GM12865	blood:	n/a	n/a
26	CTCF	chr15:76660880-76661030	GM12866	blood:	n/a	n/a
27	CTCF	chr15:76656080-76656230	MCF-7	breast:	n/a	n/a
28	CTCF	chr15:76662176-76662292	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:76697420-76697570	GM12866	blood:	n/a	n/a
30	CTCF	chr15:76662189-76662255	MCF-7	breast:	n/a	n/a
31	CTCF	chr15:76662185-76662309	MCF-7	breast:	n/a	n/a
32	CTCF	chr15:76693560-76693710	SAEC	small airway:	n/a	n/a
33	CTCF	chr15:76674220-76674370	GM12869	blood:	n/a	n/a
34	EP300	chr15:76685988-76686402	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr15:76678394-76678819	T-47D	breast:	n/a	n/a
36	EP300	chr15:76672781-76673104	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr15:76683435-76684140	T-47D	breast:	n/a	n/a
38	EP300	chr15:76683528-76684079	T-47D	breast:	n/a	n/a
39	EP300	chr15:76686003-76686352	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr15:76672483-76673245	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr15:76668220-76668927	ECC-1	luminal epithelium:	n/a	n/a
42	EP300	chr15:76682788-76683358	T-47D	breast:	n/a	chr15:76682809-76682823
43	EP300	chr15:76682775-76683264	T-47D	breast:	n/a	chr15:76682809-76682823
44	EP300	chr15:76678319-76678909	T-47D	breast:	n/a	n/a
45	EP300	chr15:76693642-76693900	Hela-S3	cervix:	n/a	n/a
46	ESR1	chr15:76682858-76683275	T-47D	breast:	n/a	n/a
47	ESR1	chr15:76682913-76683228	T-47D	breast:	n/a	n/a
48	FOS	chr15:76693663-76693948	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr15:76665186-76665277	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr15:76693689-76693922	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76692444-76692494	AG09319	gingival:	n/a
2	chr15:76692444-76692494	AG09319	gingival:	n/a
3	chr15:76669278-76669328	Caco-2	colon:	n/a
4	chr15:76669278-76669328	PrEC	prostate:	n/a
5	chr15:76669278-76669328	NH-A	brain:	n/a
6	chr15:76669278-76669328	AG09319	gingival:	n/a
7	chr15:76692444-76692494	HNPCEpiC	eye:	n/a
8	chr15:76669278-76669328	CMK	blood:	n/a
9	chr15:76669278-76669328	NHDF-neo	bronchial:	n/a
10	chr15:76692444-76692494	ovcar-3	ovarian:	n/a
11	chr15:76692444-76692494	HUVEC	blood vessel:	n/a
12	chr15:76669278-76669328	NHBE	bronchial:	n/a
13	chr15:76692444-76692494	HCF	heart:	n/a
14	chr15:76669278-76669328	HMEC	breast:	n/a
15	chr15:76669278-76669328	GM12891	blood:	n/a
16	chr15:76669278-76669328	GM12892	blood:	n/a
17	chr15:76692444-76692494	ProgFib	skin:	n/a
18	chr15:76669278-76669328	GM19239	blood:	n/a
19	chr15:76669278-76669328	HCF	heart:	n/a
20	chr15:76669278-76669328	HCPEpiC	choroid plexus:	n/a
21	chr15:76692444-76692494	BJ	skin:	n/a
22	chr15:76669278-76669328	HRPEpiC	eye:	n/a
23	chr15:76669278-76669328	HEK293	kidney:	embryo
24	chr15:76692444-76692494	AG04450	lung:	fetal
25	chr15:76669278-76669328	GM06990	blood:	n/a
26	chr15:76669278-76669328	AG10803	skin:	n/a
27	chr15:76692444-76692494	HMEC	breast:	n/a
28	chr15:76692444-76692494	GM12891	blood:	n/a
29	chr15:76669278-76669328	AG04449	skin:	fetal
30	chr15:76692444-76692494	ECC-1	luminal epithelium:	n/a
31	chr15:76669278-76669328	Jurkat	blood:	n/a
32	chr15:76692444-76692494	PrEC	prostate:	n/a
33	chr15:76669278-76669328	HRCEpiC	kidney:	n/a
34	chr15:76692444-76692494	RPTEC	kidney:	n/a
35	chr15:76692444-76692494	SK-N-MC	brain:	n/a
36	chr15:76669278-76669328	HNPCEpiC	eye:	n/a
37	chr15:76692444-76692494	Hepatocyte	liver:	n/a
38	chr15:76669278-76669328	RPTEC	kidney:	n/a
39	chr15:76692444-76692494	NHDF-neo	bronchial:	n/a
40	chr15:76692444-76692494	U87	brain:	n/a
41	chr15:76692444-76692494	HAEpiC	amniotic membrane:	n/a
42	chr15:76669278-76669328	SAEC	small airway:	n/a
43	chr15:76669278-76669328	SKMC	muscle:	n/a
44	chr15:76669278-76669328	HPAEpiC	pulmonary alveolar:	n/a
45	chr15:76669278-76669328	ovcar-3	ovarian:	n/a
46	chr15:76692444-76692494	HL-60	blood:	n/a
47	chr15:76692444-76692494	PFSK-1	brain:	n/a
48	chr15:76692444-76692494	HPAEpiC	pulmonary alveolar:	n/a
49	chr15:76692444-76692494	GM19239	blood:	n/a
50	chr15:76669278-76669328	H1-hESC	embryonic stem cell:	embryo

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76653804..76656033-chr15:76682972..76685314,2	K562	blood:
2	chr15:76630618..76633246-chr15:76671829..76673785,2	K562	blood:
3	chr15:76660945..76663101-chr15:76670042..76672423,3	MCF-7	breast:
4	chr15:76682322..76685221-chr15:76690968..76692645,2	MCF-7	breast:
5	chr15:76626949..76629326-chr15:76677792..76680688,2	MCF-7	breast:
6	chr15:76677877..76679939-chr15:76693562..76695199,2	MCF-7	breast:
7	chr15:76641041..76642748-chr15:76666424..76668885,2	K562	blood:
8	chr15:76695076..76699060-chr15:76702515..76705224,4	K562	blood:
9	chr15:76668083..76670224-chr15:76672287..76674754,2	MCF-7	breast:
10	chr15:76627109..76630617-chr15:76650461..76653550,4	MCF-7	breast:
11	chr15:76677877..76679939-chr15:76693562..76695199,2	MCF-7	breast:
12	chr15:76670479..76673232-chr15:76675468..76677243,2	MCF-7	breast:
13	chr15:76651211..76653723-chr15:76658057..76660329,2	K562	blood:
14	chr15:76655095..76656625-chr15:76656910..76658925,2	K562	blood:
15	chr15:76651115..76653988-chr15:76656127..76658474,2	MCF-7	breast:
16	chr15:76651584..76653764-chr15:76658090..76659845,2	MCF-7	breast:
17	chr15:76670479..76673232-chr15:76675468..76677243,2	MCF-7	breast:
18	chr15:76660891..76663592-chr15:76663710..76667547,3	K562	blood:
19	chr15:76669726..76672146-chr15:76676957..76678656,2	K562	blood:
20	chr15:76653804..76656033-chr15:76682972..76685314,2	K562	blood:
21	chr15:76682322..76685221-chr15:76690968..76692645,2	MCF-7	breast:
22	chr15:76634896..76638270-chr15:76657044..76660007,3	K562	blood:
23	chr15:76660945..76663101-chr15:76670042..76672423,3	MCF-7	breast:
24	chr15:76651211..76653723-chr15:76658057..76660329,2	K562	blood:
25	chr15:76654411..76657574-chr15:76660615..76665795,4	K562	blood:
26	chr15:76651584..76653764-chr15:76658090..76659845,2	MCF-7	breast:
27	chr15:76676447..76679555-chr15:76684480..76688272,4	MCF-7	breast:
28	chr15:76601775..76604028-chr15:76652704..76655186,2	K562	blood:
29	chr15:76668083..76670224-chr15:76672287..76674754,2	MCF-7	breast:
30	chr15:76655095..76656625-chr15:76656910..76658925,2	K562	blood:
31	chr15:76654411..76657574-chr15:76660615..76665795,4	K562	blood:
32	chr15:76628611..76630975-chr15:76663649..76666023,2	MCF-7	breast:
33	chr15:76660891..76663592-chr15:76663710..76667547,3	K562	blood:
34	chr15:76651115..76653988-chr15:76656127..76658474,2	MCF-7	breast:
35	chr15:76695076..76699060-chr15:76702515..76705224,4	K562	blood:
36	chr15:76654196..76656448-chr15:76658606..76661419,2	MCF-7	breast:
37	chr15:76654196..76656448-chr15:76658606..76661419,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISL2-3	chr15:76707282-76707590	ucscGeneNc_uc002bef_1
2	lnc-ISL2-3	chr15:76705751-76706962	ucscGeneNc_uc002bef_1

No data

Variant related genes	Relation type
SCAPER	TF binding region
SCAPER	CpG island
ENSG00000140386	chromatin interactions
ENSG00000270036	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000159556	chromatin interactions

Extended variants
information (count: 1831 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531218839	chr15:76653363-76653364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs74890759	chr15:76653366-76653367	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs77923587	chr15:76653377-76653378	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs78632614	chr15:76653378-76653379	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs62028375	chr15:76653380-76653381	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs533433975	chr15:76653386-76653387	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547742615	chr15:76653476-76653477	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2469223	chr15:76653477-76653478	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560479812	chr15:76653492-76653493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555696149	chr15:76653606-76653607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527688472	chr15:76653623-76653624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs8028310	chr15:76653632-76653633	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs58240508	chr15:76653639-76653640	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538560449	chr15:76653708-76653709	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138996441	chr15:76653729-76653730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373063805	chr15:76653745-76653746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537123931	chr15:76653763-76653764	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571522466	chr15:76653793-76653794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538306449	chr15:76653876-76653877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553454544	chr15:76653882-76653883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571857117	chr15:76653919-76653920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535860195	chr15:76653922-76653923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186698321	chr15:76653968-76653969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576234399	chr15:76653978-76653979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140727564	chr15:76654002-76654003	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535726920	chr15:76654013-76654014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189633509	chr15:76654140-76654141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556761482	chr15:76654164-76654165	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576611952	chr15:76654170-76654171	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538852985	chr15:76654198-76654199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377057986	chr15:76654252-76654253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545470360	chr15:76654309-76654310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111653531	chr15:76654323-76654324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs556919147	chr15:76654373-76654374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs145214186	chr15:76654407-76654408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12438257	chr15:76654416-76654417	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs137906662	chr15:76654417-76654418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201065317	chr15:76654440-76654441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572734456	chr15:76654502-76654503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs541449089	chr15:76654515-76654516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545549454	chr15:76654533-76654534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531877328	chr15:76654566-76654567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185317540	chr15:76654567-76654568	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190867418	chr15:76654604-76654605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs149483932	chr15:76654620-76654621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143915723	chr15:76654628-76654629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574863291	chr15:76654632-76654633	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183538935	chr15:76654656-76654657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186743228	chr15:76654667-76654668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569645569	chr15:76654680-76654681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76639800-76659800	Weak transcription	Gastric	stomach
2	chr15:76639800-76682600	Weak transcription	Pancreas	Pancrea
3	chr15:76639800-76695400	Weak transcription	Spleen	Spleen
4	chr15:76639800-76727400	Weak transcription	Right Ventricle	heart
5	chr15:76640200-76658800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr15:76640800-76664400	Weak transcription	Brain Angular Gyrus	brain
7	chr15:76640800-76694600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr15:76641200-76659000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr15:76641400-76694600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:76641600-76665400	Weak transcription	Placenta	Placenta
11	chr15:76641800-76660400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr15:76641800-76673400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr15:76642000-76660400	Weak transcription	Esophagus	oesophagus
14	chr15:76642200-76664400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr15:76642400-76660400	Weak transcription	Brain Hippocampus Middle	brain
16	chr15:76642800-76664600	Weak transcription	Thymus	Thymus
17	chr15:76642800-76693800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr15:76643800-76672400	Weak transcription	Primary B cells from cord blood	blood
19	chr15:76643800-76695000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr15:76644600-76664400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr15:76644600-76664600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr15:76644800-76664600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr15:76645800-76686200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:76646600-76664400	Weak transcription	Fetal Intestine Large	intestine
25	chr15:76646600-76695400	Weak transcription	Ovary	ovary
26	chr15:76646800-76659200	Weak transcription	Liver	Liver
27	chr15:76646800-76659400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr15:76646800-76666000	Weak transcription	Fetal Brain Female	brain
29	chr15:76647000-76656000	Weak transcription	Fetal Stomach	stomach
30	chr15:76647000-76660200	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:76647000-76664600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr15:76648400-76668400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr15:76648400-76674400	Weak transcription	Brain Substantia Nigra	brain
34	chr15:76648800-76659200	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr15:76649400-76659800	Weak transcription	Fetal Heart	heart
36	chr15:76650000-76660400	Weak transcription	Fetal Muscle Leg	muscle
37	chr15:76650400-76664400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr15:76650800-76674000	Weak transcription	Small Intestine	intestine
39	chr15:76651800-76659200	Weak transcription	Lung	lung
40	chr15:76652000-76658000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr15:76652000-76660400	Weak transcription	Adipose Nuclei	Adipose
42	chr15:76652200-76655600	Weak transcription	Fetal Intestine Small	intestine
43	chr15:76652200-76656600	Weak transcription	Aorta	Aorta
44	chr15:76652400-76675200	Weak transcription	Brain Germinal Matrix	brain
45	chr15:76652600-76660400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr15:76652800-76656000	Weak transcription	Primary T cells from cord blood	blood
47	chr15:76653000-76664400	Weak transcription	Left Ventricle	heart
48	chr15:76653400-76672400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr15:76655600-76657600	Strong transcription	Fetal Intestine Small	intestine
50	chr15:76656000-76656800	Strong transcription	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links