Variant report

Variant	esv3507774
Chromosome Location	chr5:15593461-15822407
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	ATF2	chr5:15796570-15797100	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:15770306-15770308	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:15604982-15605340	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:15702250-15702624	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr5:15638745-15638991	GM12878	blood:	n/a	n/a
7	BATF	chr5:15702279-15702578	GM12878	blood:	n/a	chr5:15702383-15702394 chr5:15702384-15702394 chr5:15702380-15702390
8	BCL3	chr5:15720097-15720347	GM12878	blood:	n/a	n/a
9	BCL3	chr5:15720042-15720374	GM12878	blood:	n/a	n/a
10	BCL3	chr5:15702271-15702534	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:15711672-15711674	GM12878	blood:	n/a	n/a
12	BRCA1	chr5:15650004-15650016	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr5:15809819-15810015	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr5:15655769-15655954	K562	blood:	n/a	n/a
15	CCNT2	chr5:15651809-15652005	K562	blood:	n/a	n/a
16	CEBPB	chr5:15613128-15613263	Hela-S3	cervix:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
17	CEBPB	chr5:15702151-15702351	HepG2	liver:	n/a	chr5:15702297-15702308
18	CEBPB	chr5:15634274-15634470	A549	lung:	n/a	chr5:15634380-15634391
19	CEBPB	chr5:15699969-15699981	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:15724199-15724376	A549	lung:	n/a	n/a
21	CEBPB	chr5:15611238-15611385	HepG2	liver:	n/a	chr5:15611309-15611320
22	CEBPB	chr5:15757097-15757490	IMR90	lung:	n/a	chr5:15757285-15757296 chr5:15757285-15757298 chr5:15757287-15757298
23	CEBPB	chr5:15611075-15611493	A549	lung:	n/a	chr5:15611309-15611320
24	CEBPB	chr5:15792480-15792786	IMR90	lung:	n/a	chr5:15792652-15792669 chr5:15792654-15792665
25	CEBPB	chr5:15601441-15601775	IMR90	lung:	n/a	chr5:15601603-15601614 chr5:15601603-15601616
26	CEBPB	chr5:15724155-15724432	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:15690558-15690841	HepG2	liver:	n/a	chr5:15690674-15690685
28	CEBPB	chr5:15704198-15704411	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr5:15620184-15620569	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:15601349-15601800	H1-hESC	embryonic stem cell:	n/a	chr5:15601603-15601614 chr5:15601603-15601616
31	CEBPB	chr5:15691797-15692050	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:15799216-15799445	IMR90	lung:	n/a	chr5:15799306-15799317
33	CEBPB	chr5:15613105-15613394	HepG2	liver:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
34	CEBPB	chr5:15792510-15792764	HepG2	liver:	n/a	chr5:15792652-15792669 chr5:15792654-15792665
35	CEBPB	chr5:15702226-15702347	HepG2	liver:	n/a	chr5:15702297-15702308
36	CEBPB	chr5:15702129-15702490	H1-hESC	embryonic stem cell:	n/a	chr5:15702297-15702308
37	CEBPB	chr5:15690558-15690846	A549	lung:	n/a	chr5:15690674-15690685
38	CEBPB	chr5:15680710-15680729	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:15613046-15613355	K562	blood:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234
40	CEBPB	chr5:15757243-15757366	H1-hESC	embryonic stem cell:	n/a	chr5:15757285-15757296 chr5:15757285-15757298 chr5:15757287-15757298
41	CEBPB	chr5:15748798-15748940	H1-hESC	embryonic stem cell:	n/a	chr5:15748867-15748878
42	CEBPB	chr5:15683559-15683874	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:15703479-15703722	HepG2	liver:	n/a	chr5:15703621-15703632
44	CEBPB	chr5:15821442-15821791	IMR90	lung:	n/a	n/a
45	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
46	CEBPB	chr5:15601428-15601772	HepG2	liver:	n/a	chr5:15601603-15601614 chr5:15601603-15601616
47	CEBPB	chr5:15748747-15749013	IMR90	lung:	n/a	chr5:15748867-15748878
48	CEBPB	chr5:15799193-15799390	A549	lung:	n/a	chr5:15799306-15799317
49	CEBPB	chr5:15638600-15638721	HepG2	liver:	n/a	chr5:15638648-15638665 chr5:15638651-15638664 chr5:15638653-15638664 chr5:15638651-15638662 chr5:15638653-15638664 chr5:15638651-15638664
50	CEBPB	chr5:15613104-15613366	A549	lung:	n/a	chr5:15613221-15613232 chr5:15613221-15613234 chr5:15613223-15613232 chr5:15613223-15613234

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:15692835-15692885	AG04449	skin:	fetal
2	chr5:15692835-15692885	AG04449	skin:	fetal
3	chr5:15692835-15692885	GM12892	blood:	n/a
4	chr5:15683259-15683309	SK-N-MC	brain:	n/a
5	chr5:15683259-15683309	HRCEpiC	kidney:	n/a
6	chr5:15683259-15683309	HEEpiC	esophagus:	n/a
7	chr5:15757078-15757128	Hepatocyte	liver:	n/a
8	chr5:15720153-15720203	Hepatocyte	liver:	n/a
9	chr5:15720153-15720203	HUVEC	blood vessel:	n/a
10	chr5:15737401-15737451	AG09309	skin:	n/a
11	chr5:15694721-15694771	HAEpiC	amniotic membrane:	n/a
12	chr5:15720153-15720203	GM12891	blood:	n/a
13	chr5:15595186-15595236	Jurkat	blood:	n/a
14	chr5:15737401-15737451	GM19239	blood:	n/a
15	chr5:15737401-15737451	H1-hESC	embryonic stem cell:	embryo
16	chr5:15683259-15683309	AG04450	lung:	fetal
17	chr5:15645642-15645692	HCPEpiC	choroid plexus:	n/a
18	chr5:15595186-15595236	HIPEpiC	eye:	n/a
19	chr5:15737401-15737451	K562	blood:	n/a
20	chr5:15692835-15692885	MCF10A-Er-Src	breast:	n/a
21	chr5:15750836-15750886	RPTEC	kidney:	n/a
22	chr5:15737401-15737451	ovcar-3	ovarian:	n/a
23	chr5:15694721-15694771	AoSMC	blood vessel:	n/a
24	chr5:15645642-15645692	NHBE	bronchial:	n/a
25	chr5:15757078-15757128	HNPCEpiC	eye:	n/a
26	chr5:15683259-15683309	K562	blood:	n/a
27	chr5:15720153-15720203	AG09319	gingival:	n/a
28	chr5:15720153-15720203	AG04449	skin:	fetal
29	chr5:15595186-15595236	HUVEC	blood vessel:	n/a
30	chr5:15692835-15692885	HL-60	blood:	n/a
31	chr5:15595186-15595236	MCF10A-Er-Src	breast:	n/a
32	chr5:15757078-15757128	PFSK-1	brain:	n/a
33	chr5:15757078-15757128	NH-A	brain:	n/a
34	chr5:15645642-15645692	HRE	kidney:	n/a
35	chr5:15757078-15757128	GM12892	blood:	n/a
36	chr5:15692835-15692885	NH-A	brain:	n/a
37	chr5:15683259-15683309	HL-60	blood:	n/a
38	chr5:15750836-15750886	HUVEC	blood vessel:	n/a
39	chr5:15720153-15720203	K562	blood:	n/a
40	chr5:15750836-15750886	GM12878	blood:	n/a
41	chr5:15720153-15720203	PrEC	prostate:	n/a
42	chr5:15694721-15694771	T-47D	breast:	n/a
43	chr5:15750836-15750886	HMEC	breast:	n/a
44	chr5:15595186-15595236	Caco-2	colon:	n/a
45	chr5:15692835-15692885	HepG2	liver:	n/a
46	chr5:15757078-15757128	HCM	heart:	n/a
47	chr5:15595186-15595236	HAEpiC	amniotic membrane:	n/a
48	chr5:15750836-15750886	HIPEpiC	eye:	n/a
49	chr5:15694721-15694771	SAEC	small airway:	n/a
50	chr5:15645642-15645692	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:147603707..147604442-chr5:15685536..15686251,2	MCF-7	breast:
2	chr5:15719277..15719777-chr8:33370846..33371373,2	Hela-S3	cervix:
3	chr5:15105857..15106576-chr5:15791048..15791750,2	MCF-7	breast:
4	chr5:15463054..15463835-chr5:15793947..15794638,2	MCF-7	breast:
5	chr5:15804150..15805697-chr5:15806057..15808758,2	K562	blood:
6	chr5:15463040..15463892-chr5:15794004..15794911,3	MCF-7	breast:
7	chr5:15691207..15693876-chr5:15698019..15699867,2	K562	blood:
8	chr5:15611811..15614735-chr5:15615053..15617444,2	K562	blood:
9	chr5:15747913..15750874-chr5:15750994..15753003,2	K562	blood:
10	chr3:137893053..137895018-chr5:15659439..15660939,2	MCF-7	breast:
11	chr5:15683076..15684017-chr5:15995401..15996222,3	MCF-7	breast:
12	chr5:15691412..15693844-chr5:15721863..15723411,2	MCF-7	breast:
13	chr5:15804197..15806125-chr5:15806935..15808758,2	K562	blood:
14	chr5:15383237..15384294-chr5:15793976..15794826,3	MCF-7	breast:
15	chr5:15691412..15693844-chr5:15721863..15723411,2	MCF-7	breast:
16	chr5:15747913..15750874-chr5:15750994..15753003,2	K562	blood:
17	chr5:15691207..15693876-chr5:15698019..15699867,2	K562	blood:
18	chr5:15804150..15805697-chr5:15806057..15808758,2	K562	blood:
19	chr5:15804197..15806125-chr5:15806935..15808758,2	K562	blood:

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

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

Extended variants
information (count: 8926 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:8926 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570283367	chr5:15593498-15593499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140490373	chr5:15593552-15593553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555999538	chr5:15593555-15593556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574647460	chr5:15593564-15593565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542151865	chr5:15593587-15593588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572851078	chr5:15593658-15593659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540577717	chr5:15593684-15593685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572039914	chr5:15593696-15593697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190952960	chr5:15593715-15593716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183092232	chr5:15593724-15593725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532714821	chr5:15593821-15593822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544825943	chr5:15593851-15593852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573849036	chr5:15593883-15593884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530318953	chr5:15593886-15593887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146754686	chr5:15593907-15593908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566732524	chr5:15593909-15593910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559168717	chr5:15593944-15593945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148903359	chr5:15593948-15593949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549878276	chr5:15593974-15593975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187600818	chr5:15593976-15593977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570621185	chr5:15594026-15594027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537602458	chr5:15594063-15594064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556082178	chr5:15594073-15594074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568283147	chr5:15594074-15594075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192798093	chr5:15594117-15594118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554060074	chr5:15594187-15594188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541248949	chr5:15594204-15594205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143528152	chr5:15594265-15594266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545825549	chr5:15594268-15594269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577387929	chr5:15594309-15594310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571507639	chr5:15594315-15594316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62347907	chr5:15594327-15594328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557842617	chr5:15594374-15594375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539024117	chr5:15594404-15594405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150987653	chr5:15594518-15594519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543583034	chr5:15594533-15594534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562925723	chr5:15594534-15594535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528719663	chr5:15594549-15594550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553777351	chr5:15594557-15594558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575007098	chr5:15594558-15594559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542130747	chr5:15594559-15594560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182515025	chr5:15594568-15594569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188375898	chr5:15594569-15594570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552155527	chr5:15594582-15594583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140761998	chr5:15594618-15594619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17601401	chr5:15594620-15594621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553594981	chr5:15594642-15594643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550280990	chr5:15594664-15594665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12516253	chr5:15594674-15594675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565546982	chr5:15594677-15594678	Weak transcription Enhancers	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:2599 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15574000-15594200	Weak transcription	Fetal Kidney	kidney
2	chr5:15578200-15596200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:15578200-15600200	Weak transcription	Left Ventricle	heart
4	chr5:15581000-15604400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr5:15581600-15603400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr5:15584000-15599200	Weak transcription	HSMMtube	muscle
7	chr5:15585000-15594600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:15585000-15604000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr5:15585000-15606400	Weak transcription	Adipose Nuclei	Adipose
10	chr5:15585000-15630200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr5:15585200-15594200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:15585200-15594400	Weak transcription	Fetal Muscle Leg	muscle
13	chr5:15585200-15600000	Weak transcription	HSMM	muscle
14	chr5:15585200-15601000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr5:15585200-15602000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr5:15585200-15605200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr5:15585800-15594600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:15586000-15619800	Weak transcription	NHLF	lung
19	chr5:15586400-15598800	Weak transcription	Aorta	Aorta
20	chr5:15587400-15596600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr5:15587400-15600200	Weak transcription	Lung	lung
22	chr5:15587800-15601000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr5:15587800-15601000	Weak transcription	Brain Anterior Caudate	brain
24	chr5:15588200-15598200	Weak transcription	Colon Smooth Muscle	Colon
25	chr5:15588200-15598800	Weak transcription	Brain Substantia Nigra	brain
26	chr5:15588200-15605400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:15588400-15600400	Weak transcription	Brain Hippocampus Middle	brain
28	chr5:15588400-15612600	Weak transcription	NHDF-Ad	bronchial
29	chr5:15588800-15603600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:15590800-15605000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:15592200-15593600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr5:15592200-15593600	Enhancers	Ovary	ovary
33	chr5:15592400-15593600	Enhancers	Fetal Stomach	stomach
34	chr5:15592400-15593800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:15593200-15594400	Weak transcription	Fetal Heart	heart
36	chr5:15593400-15594400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:15593400-15606000	Weak transcription	HUVEC	blood vessel
38	chr5:15593400-15633400	Weak transcription	Fetal Lung	lung
39	chr5:15593600-15594400	Weak transcription	Ovary	ovary
40	chr5:15593600-15600000	Weak transcription	Fetal Stomach	stomach
41	chr5:15593600-15606200	Weak transcription	Fetal Brain Male	brain
42	chr5:15593600-15606400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr5:15593800-15601000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:15594200-15594600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:15594200-15595000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:15594200-15595200	Enhancers	Fetal Kidney	kidney
47	chr5:15594400-15595200	Enhancers	Ovary	ovary
48	chr5:15594400-15595400	Enhancers	Fetal Muscle Leg	muscle
49	chr5:15594400-15595600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:15594400-15596000	Enhancers	HUES64 Cell Line	embryonic stem cell

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