Variant report

Variant	nsv830214
Chromosome Location	chr5:15589809-15791032
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	ATF1	chr5:15762325-15762618	K562	blood:	n/a	n/a
2	BACH1	chr5:15770306-15770308	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:15702250-15702624	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:15604982-15605340	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr5:15702279-15702578	GM12878	blood:	n/a	chr5:15702383-15702394 chr5:15702384-15702394 chr5:15702380-15702390
6	BATF	chr5:15638745-15638991	GM12878	blood:	n/a	n/a
7	BCL3	chr5:15720042-15720374	GM12878	blood:	n/a	n/a
8	BCL3	chr5:15720097-15720347	GM12878	blood:	n/a	n/a
9	BCL3	chr5:15702271-15702534	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:15711672-15711674	GM12878	blood:	n/a	n/a
11	BRCA1	chr5:15650004-15650016	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr5:15651809-15652005	K562	blood:	n/a	n/a
13	CCNT2	chr5:15655769-15655954	K562	blood:	n/a	n/a
14	CEBPB	chr5:15748747-15749013	IMR90	lung:	n/a	chr5:15748867-15748878
15	CEBPB	chr5:15601428-15601772	HepG2	liver:	n/a	chr5:15601603-15601614 chr5:15601603-15601616
16	CEBPB	chr5:15680710-15680729	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:15683559-15683874	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:15703479-15703722	HepG2	liver:	n/a	chr5:15703621-15703632
19	CEBPB	chr5:15737565-15737906	HepG2	liver:	n/a	chr5:15737715-15737724 chr5:15737715-15737726 chr5:15737715-15737724 chr5:15737713-15737726 chr5:15737715-15737724 chr5:15737715-15737724 chr5:15737713-15737724
20	CEBPB	chr5:15704198-15704411	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:15601349-15601800	H1-hESC	embryonic stem cell:	n/a	chr5:15601603-15601614 chr5:15601603-15601616
22	CEBPB	chr5:15611120-15611498	K562	blood:	n/a	chr5:15611309-15611320
23	CEBPB	chr5:15737584-15737878	A549	lung:	n/a	chr5:15737715-15737724 chr5:15737715-15737726 chr5:15737715-15737724 chr5:15737713-15737726 chr5:15737715-15737724 chr5:15737715-15737724 chr5:15737713-15737724
24	CEBPB	chr5:15613128-15613263	Hela-S3	cervix:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
25	CEBPB	chr5:15644483-15644633	HepG2	liver:	n/a	chr5:15644534-15644545
26	CEBPB	chr5:15611238-15611385	HepG2	liver:	n/a	chr5:15611309-15611320
27	CEBPB	chr5:15702151-15702351	HepG2	liver:	n/a	chr5:15702297-15702308
28	CEBPB	chr5:15611066-15611546	MCF-7	breast:	n/a	chr5:15611309-15611320
29	CEBPB	chr5:15611129-15611499	HepG2	liver:	n/a	chr5:15611309-15611320
30	CEBPB	chr5:15690558-15690841	HepG2	liver:	n/a	chr5:15690674-15690685
31	CEBPB	chr5:15690490-15690972	IMR90	lung:	n/a	chr5:15690674-15690685
32	CEBPB	chr5:15644498-15644627	H1-hESC	embryonic stem cell:	n/a	chr5:15644534-15644545
33	CEBPB	chr5:15613105-15613394	HepG2	liver:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
34	CEBPB	chr5:15601441-15601775	IMR90	lung:	n/a	chr5:15601603-15601614 chr5:15601603-15601616
35	CEBPB	chr5:15611075-15611493	A549	lung:	n/a	chr5:15611309-15611320
36	CEBPB	chr5:15724155-15724432	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:15634221-15634421	HepG2	liver:	n/a	chr5:15634380-15634391
38	CEBPB	chr5:15611179-15611411	ECC-1	luminal epithelium:	n/a	chr5:15611309-15611320
39	CEBPB	chr5:15611127-15611503	A549	lung:	n/a	chr5:15611309-15611320
40	CEBPB	chr5:15740506-15740860	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:15620184-15620569	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:15757132-15757409	A549	lung:	n/a	chr5:15757285-15757296 chr5:15757285-15757298 chr5:15757287-15757298
43	CEBPB	chr5:15613058-15613413	IMR90	lung:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
44	CEBPB	chr5:15611127-15611528	H1-hESC	embryonic stem cell:	n/a	chr5:15611309-15611320
45	CEBPB	chr5:15590683-15590789	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:15611124-15611505	IMR90	lung:	n/a	chr5:15611309-15611320
47	CEBPB	chr5:15724199-15724376	A549	lung:	n/a	n/a
48	CEBPB	chr5:15613104-15613366	A549	lung:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
49	CEBPB	chr5:15691797-15692050	IMR90	lung:	n/a	n/a
50	CEBPB	chr5:15748824-15748925	K562	blood:	n/a	chr5:15748867-15748878

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:15750836-15750886	SAEC	small airway:	n/a
2	chr5:15750836-15750886	SAEC	small airway:	n/a
3	chr5:15692835-15692885	LNCaP	prostate:	n/a
4	chr5:15595186-15595236	Jurkat	blood:	n/a
5	chr5:15750836-15750886	LNCaP	prostate:	n/a
6	chr5:15757078-15757128	SK-N-SH_RA	brain:	n/a
7	chr5:15737401-15737451	NHDF-neo	bronchial:	n/a
8	chr5:15694721-15694771	HEK293	kidney:	embryo
9	chr5:15683259-15683309	CMK	blood:	n/a
10	chr5:15683259-15683309	GM12891	blood:	n/a
11	chr5:15737401-15737451	Caco-2	colon:	n/a
12	chr5:15737401-15737451	HepG2	liver:	n/a
13	chr5:15694721-15694771	RPTEC	kidney:	n/a
14	chr5:15737401-15737451	PANC-1	pancreas:	n/a
15	chr5:15683259-15683309	HRPEpiC	eye:	n/a
16	chr5:15595186-15595236	U87	brain:	n/a
17	chr5:15750836-15750886	T-47D	breast:	n/a
18	chr5:15692835-15692885	BJ	skin:	n/a
19	chr5:15694721-15694771	AG04449	skin:	fetal
20	chr5:15757078-15757128	Caco-2	colon:	n/a
21	chr5:15683259-15683309	HNPCEpiC	eye:	n/a
22	chr5:15694721-15694771	BE2_C	brain:	n/a
23	chr5:15645642-15645692	SKMC	muscle:	n/a
24	chr5:15645642-15645692	HNPCEpiC	eye:	n/a
25	chr5:15737401-15737451	NHBE	bronchial:	n/a
26	chr5:15720153-15720203	SK-N-SH_RA	brain:	n/a
27	chr5:15645642-15645692	ProgFib	skin:	n/a
28	chr5:15737401-15737451	AG09319	gingival:	n/a
29	chr5:15595186-15595236	RPTEC	kidney:	n/a
30	chr5:15757078-15757128	GM06990	blood:	n/a
31	chr5:15683259-15683309	T-47D	breast:	n/a
32	chr5:15750836-15750886	U87	brain:	n/a
33	chr5:15757078-15757128	ProgFib	skin:	n/a
34	chr5:15757078-15757128	AoSMC	blood vessel:	n/a
35	chr5:15737401-15737451	PFSK-1	brain:	n/a
36	chr5:15757078-15757128	T-47D	breast:	n/a
37	chr5:15683259-15683309	IMR90	lung:	fetal
38	chr5:15595186-15595236	ECC-1	luminal epithelium:	n/a
39	chr5:15595186-15595236	HCT-116	colon:	n/a
40	chr5:15757078-15757128	U87	brain:	n/a
41	chr5:15757078-15757128	Jurkat	blood:	n/a
42	chr5:15692835-15692885	NH-A	brain:	n/a
43	chr5:15737401-15737451	U87	brain:	n/a
44	chr5:15757078-15757128	HepG2	liver:	n/a
45	chr5:15645642-15645692	H1-hESC	embryonic stem cell:	embryo
46	chr5:15683259-15683309	SKMC	muscle:	n/a
47	chr5:15720153-15720203	HRPEpiC	eye:	n/a
48	chr5:15645642-15645692	AG09319	gingival:	n/a
49	chr5:15692835-15692885	SK-N-SH	brain:	n/a
50	chr5:15683259-15683309	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:15691207..15693876-chr5:15698019..15699867,2	K562	blood:
2	chr5:15691412..15693844-chr5:15721863..15723411,2	MCF-7	breast:
3	chr5:15747913..15750874-chr5:15750994..15753003,2	K562	blood:
4	chr5:15611811..15614735-chr5:15615053..15617444,2	K562	blood:
5	chr5:15747913..15750874-chr5:15750994..15753003,2	K562	blood:
6	chr5:15691207..15693876-chr5:15698019..15699867,2	K562	blood:
7	chr5:15719277..15719777-chr8:33370846..33371373,2	Hela-S3	cervix:
8	chr3:137893053..137895018-chr5:15659439..15660939,2	MCF-7	breast:
9	chr5:15683076..15684017-chr5:15995401..15996222,3	MCF-7	breast:
10	chr4:147603707..147604442-chr5:15685536..15686251,2	MCF-7	breast:
11	chr5:15691412..15693844-chr5:15721863..15723411,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCH11-2	chr5:15615085-15615111	NR_109945
2	lnc-MARCH11-2	chr5:15607269-15607457	ENSG00000250250.1
3	lnc-FAM105B-10	chr5:15675993-15677600	NONHSAT100586
4	lnc-MARCH11-2	chr5:15606869-15607140	ENSG00000250250.1
5	lnc-MARCH11-2	chr5:15607269-15607358	ENSG00000250250.1
6	lnc-MARCH11-2	chr5:15602298-15602468	NR_109945
7	lnc-MARCH11-2	chr5:15614727-15614996	NONHSAT100585
8	lnc-MARCH11-2	chr5:15615085-15615268	NONHSAT100585
9	lnc-MARCH11-2	chr5:15607269-15607455	NR_109945
10	lnc-FAM105B-11	chr5:15775820-15777145	NONHSAT100587
11	lnc-MARCH11-2	chr5:15602298-15602468	ENSG00000250250.1

Variant related genes	Relation type
FBXL7	TF binding region
ENSG00000250250	TF binding region
FBXL7	CpG island
ENSG00000250250	CpG island
ENSG00000129696	chromatin interactions
ENSG00000183580	chromatin interactions
ENSG00000239039	chromatin interactions
ENSG00000138231	chromatin interactions

Extended variants
information (count: 7836 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7836 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566911054	chr5:15589835-15589836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557924383	chr5:15589844-15589845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7732619	chr5:15589895-15589896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs10520818	chr5:15589917-15589918	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs567462113	chr5:15589947-15589948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562428235	chr5:15589962-15589963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573918325	chr5:15590031-15590032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146790587	chr5:15590052-15590053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559542212	chr5:15590082-15590083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186536665	chr5:15590107-15590108	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376303939	chr5:15590165-15590166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554251308	chr5:15590170-15590171	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141081365	chr5:15590203-15590204	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530753078	chr5:15590249-15590250	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192727820	chr5:15590269-15590270	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369308595	chr5:15590304-15590305	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368121570	chr5:15590321-15590322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371987197	chr5:15590336-15590337	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11960780	chr5:15590404-15590405	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs79204008	chr5:15590409-15590410	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs546575758	chr5:15590417-15590418	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs571198960	chr5:15590427-15590428	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs116510530	chr5:15590477-15590478	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs556668023	chr5:15590485-15590486	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs185075857	chr5:15590494-15590495	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs138775195	chr5:15590503-15590504	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs555743743	chr5:15590547-15590548	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs574278247	chr5:15590581-15590582	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77231038	chr5:15590631-15590632	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189537002	chr5:15590643-15590644	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs578095346	chr5:15590645-15590646	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4702086	chr5:15590727-15590728	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs563793647	chr5:15590751-15590752	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140335150	chr5:15590754-15590755	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112734907	chr5:15590772-15590773	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560974944	chr5:15590794-15590795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201280926	chr5:15590962-15590963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556166694	chr5:15591000-15591001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577986594	chr5:15591041-15591042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138125646	chr5:15591069-15591070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150361531	chr5:15591077-15591078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571203223	chr5:15591110-15591111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193189241	chr5:15591122-15591123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184450227	chr5:15591123-15591124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568621696	chr5:15591128-15591129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34971092	chr5:15591136-15591137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562541001	chr5:15591188-15591189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189562218	chr5:15591190-15591191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555925779	chr5:15591264-15591265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200337312	chr5:15591272-15591273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2252 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15574000-15594200	Weak transcription	Fetal Kidney	kidney
2	chr5:15578200-15590200	Weak transcription	Right Ventricle	heart
3	chr5:15578200-15596200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr5:15578200-15600200	Weak transcription	Left Ventricle	heart
5	chr5:15581000-15604400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr5:15581600-15603400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr5:15584000-15599200	Weak transcription	HSMMtube	muscle
8	chr5:15585000-15594600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:15585000-15604000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr5:15585000-15606400	Weak transcription	Adipose Nuclei	Adipose
11	chr5:15585000-15630200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:15585200-15594200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:15585200-15594400	Weak transcription	Fetal Muscle Leg	muscle
14	chr5:15585200-15600000	Weak transcription	HSMM	muscle
15	chr5:15585200-15601000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr5:15585200-15602000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:15585200-15605200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr5:15585800-15594600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr5:15586000-15619800	Weak transcription	NHLF	lung
20	chr5:15586400-15598800	Weak transcription	Aorta	Aorta
21	chr5:15586800-15592800	Weak transcription	Fetal Lung	lung
22	chr5:15587400-15592400	Weak transcription	Fetal Stomach	stomach
23	chr5:15587400-15596600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:15587400-15600200	Weak transcription	Lung	lung
25	chr5:15587600-15590000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr5:15587800-15601000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr5:15587800-15601000	Weak transcription	Brain Anterior Caudate	brain
28	chr5:15588200-15590000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:15588200-15592400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:15588200-15598200	Weak transcription	Colon Smooth Muscle	Colon
31	chr5:15588200-15598800	Weak transcription	Brain Substantia Nigra	brain
32	chr5:15588200-15605400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:15588400-15592200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr5:15588400-15592200	Weak transcription	Ovary	ovary
35	chr5:15588400-15600400	Weak transcription	Brain Hippocampus Middle	brain
36	chr5:15588400-15612600	Weak transcription	NHDF-Ad	bronchial
37	chr5:15588800-15590400	Enhancers	Fetal Heart	heart
38	chr5:15588800-15603600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:15590000-15590600	Enhancers	Brain Cingulate Gyrus	brain
40	chr5:15590000-15590800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:15590000-15591200	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr5:15590200-15590800	Enhancers	Right Ventricle	heart
43	chr5:15590400-15590600	Flanking Active TSS	Fetal Heart	heart
44	chr5:15590600-15591000	Enhancers	Fetal Heart	heart
45	chr5:15590800-15605000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:15591000-15592200	Weak transcription	Fetal Heart	heart
47	chr5:15592200-15593200	Enhancers	Fetal Heart	heart
48	chr5:15592200-15593600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr5:15592200-15593600	Enhancers	Ovary	ovary
50	chr5:15592400-15593600	Enhancers	Fetal Stomach	stomach

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