Variant report

Variant	nsv1021530
Chromosome Location	chr5:111626266-111683317
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	BCL3	chr5:111627738-111628008	GM12878	blood:	n/a	n/a
2	BHLHE40	chr5:111672660-111672866	HepG2	liver:	n/a	chr5:111672779-111672800 chr5:111672784-111672793 chr5:111672783-111672796 chr5:111672785-111672794
3	BHLHE40	chr5:111665513-111665737	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:111674313-111675097	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:111649518-111649702	K562	blood:	n/a	n/a
6	CEBPB	chr5:111648588-111648889	IMR90	lung:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
7	CEBPB	chr5:111674735-111675013	A549	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
8	CEBPB	chr5:111674684-111675000	IMR90	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
9	CEBPB	chr5:111674386-111675014	A549	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
10	CEBPB	chr5:111674572-111675011	H1-hESC	embryonic stem cell:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
11	CEBPB	chr5:111664552-111664647	HepG2	liver:	n/a	chr5:111664599-111664610
12	CEBPB	chr5:111674335-111675109	ECC-1	luminal epithelium:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
13	CEBPB	chr5:111674223-111675149	Hela-S3	cervix:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
14	CEBPB	chr5:111674383-111675019	HepG2	liver:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
15	CEBPB	chr5:111674221-111675111	ECC-1	luminal epithelium:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
16	CEBPB	chr5:111649599-111649624	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:111674743-111674884	HepG2	liver:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
18	CEBPB	chr5:111648598-111648854	HepG2	liver:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
19	CEBPB	chr5:111674734-111674998	K562	blood:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
20	CEBPB	chr5:111648622-111648781	K562	blood:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
21	CEBPB	chr5:111672672-111672946	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:111674347-111675076	MCF-7	breast:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
23	CEBPB	chr5:111648572-111648903	A549	lung:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
24	CEBPB	chr5:111647976-111648996	Hela-S3	cervix:	n/a	chr5:111648694-111648711 chr5:111648118-111648131 chr5:111648696-111648707 chr5:111648437-111648448
25	CEBPB	chr5:111648529-111648917	A549	lung:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
26	CEBPB	chr5:111644377-111644795	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr5:111648486-111648956	ECC-1	luminal epithelium:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
28	CEBPB	chr5:111674312-111675089	A549	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
29	CEBPB	chr5:111674525-111675177	MCF-7	breast:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
30	CEBPB	chr5:111660737-111660943	IMR90	lung:	n/a	n/a
31	CEBPB	chr5:111674424-111675026	K562	blood:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
32	CEBPB	chr5:111660740-111660940	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:111648479-111648970	ECC-1	luminal epithelium:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
34	CHD2	chr5:111674287-111675069	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr5:111638538-111638571	ProgFib	skin:	n/a	n/a
36	CTCF	chr5:111652461-111652566	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:111630595-111630773	GM12878	blood:	n/a	n/a
38	CTCF	chr5:111637280-111637430	A549	lung:	n/a	n/a
39	CTCF	chr5:111637340-111637490	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr5:111637422-111637425	LNCaP	prostate:	n/a	n/a
41	CTCF	chr5:111652500-111652650	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:111630600-111630793	K562	blood:	n/a	n/a
43	CTCF	chr5:111652580-111652730	RPTEC	kidney:	n/a	n/a
44	CTCF	chr5:111630620-111630770	RPTEC	kidney:	n/a	n/a
45	CTCF	chr5:111630597-111630717	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:111637345-111637407	K562	blood:	n/a	n/a
47	CTCF	chr5:111630600-111630750	RPTEC	kidney:	n/a	n/a
48	CTCF	chr5:111637300-111637450	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr5:111652400-111652550	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:111652427-111652570	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:111665548-111665598	NB4	blood:	n/a
2	chr5:111665548-111665598	AG09319	gingival:	n/a
3	chr5:111665548-111665598	HEEpiC	esophagus:	n/a
4	chr5:111665548-111665598	AG09309	skin:	n/a
5	chr5:111665548-111665598	NH-A	brain:	n/a
6	chr5:111665548-111665598	GM12891	blood:	n/a
7	chr5:111665548-111665598	K562	blood:	n/a
8	chr5:111665548-111665598	GM12892	blood:	n/a
9	chr5:111665548-111665598	SK-N-SH_RA	brain:	n/a
10	chr5:111665548-111665598	AoSMC	blood vessel:	n/a
11	chr5:111665548-111665598	HL-60	blood:	n/a
12	chr5:111665548-111665598	HCT-116	colon:	n/a
13	chr5:111665548-111665598	HCM	heart:	n/a
14	chr5:111665548-111665598	SK-N-MC	brain:	n/a
15	chr5:111665548-111665598	CMK	blood:	n/a
16	chr5:111665548-111665598	Caco-2	colon:	n/a
17	chr5:111665548-111665598	GM19239	blood:	n/a
18	chr5:111665548-111665598	NT2-D1	testis:	n/a
19	chr5:111665548-111665598	HNPCEpiC	eye:	n/a
20	chr5:111665548-111665598	SK-N-SH	brain:	n/a
21	chr5:111665548-111665598	U87	brain:	n/a
22	chr5:111665548-111665598	BJ	skin:	n/a
23	chr5:111665548-111665598	HCF	heart:	n/a
24	chr5:111665548-111665598	HepG2	liver:	n/a
25	chr5:111665548-111665598	HMEC	breast:	n/a
26	chr5:111665548-111665598	SKMC	muscle:	n/a
27	chr5:111665548-111665598	NHDF-neo	bronchial:	n/a
28	chr5:111665548-111665598	HAEpiC	amniotic membrane:	n/a
29	chr5:111665548-111665598	PrEC	prostate:	n/a
30	chr5:111665548-111665598	BE2_C	brain:	n/a
31	chr5:111665548-111665598	Hepatocyte	liver:	n/a
32	chr5:111665548-111665598	RPTEC	kidney:	n/a
33	chr5:111665548-111665598	HUVEC	blood vessel:	n/a
34	chr5:111665548-111665598	GM12878	blood:	n/a
35	chr5:111665548-111665598	T-47D	breast:	n/a
36	chr5:111665548-111665598	Jurkat	blood:	n/a
37	chr5:111665548-111665598	A549	lung:	n/a
38	chr5:111665548-111665598	MCF10A-Er-Src	breast:	n/a
39	chr5:111665548-111665598	H1-hESC	embryonic stem cell:	embryo
40	chr5:111665548-111665598	AG04450	lung:	fetal
41	chr5:111665548-111665598	GM06990	blood:	n/a
42	chr5:111665548-111665598	HRPEpiC	eye:	n/a
43	chr5:111665548-111665598	ECC-1	luminal epithelium:	n/a
44	chr5:111665548-111665598	Hela-S3	cervix:	n/a
45	chr5:111665548-111665598	IMR90	lung:	fetal
46	chr5:111665548-111665598	HRE	kidney:	n/a
47	chr5:111665548-111665598	AG04449	skin:	fetal
48	chr5:111665548-111665598	HCPEpiC	choroid plexus:	n/a
49	chr5:111665548-111665598	MCF-7	breast:	n/a
50	chr5:111665548-111665598	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:111676724..111678269-chr5:111678976..111680650,2	MCF-7	breast:
2	chr5:111664622..111667062-chr5:111669246..111671249,2	K562	blood:
3	chr5:111678130..111679875-chr5:111682477..111684112,2	K562	blood:
4	chr5:111642905..111645831-chr5:111648722..111651593,3	K562	blood:
5	chr5:111496502..111498084-chr5:111652901..111655234,2	MCF-7	breast:
6	chr5:111664622..111667062-chr5:111669246..111671249,2	K562	blood:
7	chr5:111681506..111684177-chr5:111711327..111713137,2	K562	blood:
8	chr5:111676724..111678269-chr5:111678976..111680650,2	MCF-7	breast:
9	chr5:111629073..111631228-chr5:111635645..111639350,3	K562	blood:
10	chr5:111625117..111627783-chr5:111753976..111755871,2	MCF-7	breast:
11	chr5:111654503..111657162-chr5:111657627..111659825,2	K562	blood:
12	chr5:111629073..111631228-chr5:111635645..111639350,3	K562	blood:
13	chr5:111678130..111679875-chr5:111682477..111684112,2	K562	blood:
14	chr5:111638084..111640308-chr5:111646622..111650517,3	K562	blood:
15	chr5:111638084..111640308-chr5:111646622..111650517,3	K562	blood:
16	chr5:111654503..111657162-chr5:111657627..111659825,2	K562	blood:
17	chr5:111672466..111674712-chr5:111689508..111691131,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf13-5	chr5:111643083-111643099	NONHSAT103225

Variant related genes	Relation type
EPB41L4A	TF binding region
EPB41L4A	CpG island
ENSG00000129595	chromatin interactions
ENSG00000268358	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000238363	chromatin interactions

Extended variants
information (count: 2375 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2375 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17164116	chr5:111626266-111626267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs1524427	chr5:111626273-111626274	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191917872	chr5:111626316-111626317	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184039212	chr5:111626324-111626325	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563354526	chr5:111626365-111626366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs530842054	chr5:111626405-111626406	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142077969	chr5:111626505-111626506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs60977105	chr5:111626525-111626526	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs4455607	chr5:111626532-111626533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs547224176	chr5:111626608-111626609	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568723811	chr5:111626612-111626613	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs75077126	chr5:111626616-111626617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs151133532	chr5:111626714-111626715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs79492686	chr5:111626781-111626782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139579704	chr5:111626790-111626791	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557825680	chr5:111626860-111626861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566456051	chr5:111626889-111626890	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs533696307	chr5:111626935-111626936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs17269764	chr5:111626954-111626955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs115858286	chr5:111627015-111627016	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs192640640	chr5:111627022-111627023	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs73788246	chr5:111627047-111627048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs370077907	chr5:111627061-111627062	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs575589490	chr5:111627114-111627115	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545917034	chr5:111627166-111627167	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115211668	chr5:111627187-111627188	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528598996	chr5:111627223-111627224	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs540801888	chr5:111627265-111627266	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56332921	chr5:111627271-111627272	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs544108155	chr5:111627272-111627273	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374090819	chr5:111627382-111627383	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564695795	chr5:111627448-111627449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs59723280	chr5:111627475-111627476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs551293921	chr5:111627491-111627492	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147586722	chr5:111627502-111627503	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs67586008	chr5:111627517-111627518	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs184618180	chr5:111627561-111627562	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566537299	chr5:111627580-111627581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs567936366	chr5:111627601-111627602	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533660619	chr5:111627602-111627603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548700170	chr5:111627609-111627610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189136902	chr5:111627619-111627620	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs142220981	chr5:111627636-111627637	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541085916	chr5:111627668-111627669	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs115357055	chr5:111627675-111627676	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149714127	chr5:111627691-111627692	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116712147	chr5:111627694-111627695	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs145660333	chr5:111627713-111627714	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573341248	chr5:111627804-111627805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540708708	chr5:111627805-111627806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Prostate cancer	22341455	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111586600-111626400	Weak transcription	Gastric	stomach
2	chr5:111590400-111628200	Weak transcription	Aorta	Aorta
3	chr5:111620600-111626400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:111625000-111628400	Enhancers	Fetal Heart	heart
5	chr5:111625600-111626800	Weak transcription	Left Ventricle	heart
6	chr5:111625800-111626400	Weak transcription	Lung	lung
7	chr5:111626200-111627000	Enhancers	Right Atrium	heart
8	chr5:111626400-111626600	Enhancers	Placenta Amnion	Placenta Amnion
9	chr5:111626400-111627400	Enhancers	Gastric	stomach
10	chr5:111626800-111628000	Enhancers	Left Ventricle	heart
11	chr5:111626800-111628000	Enhancers	Right Ventricle	heart
12	chr5:111627000-111629400	Weak transcription	Right Atrium	heart
13	chr5:111627400-111630000	Weak transcription	Gastric	stomach
14	chr5:111628000-111629200	Weak transcription	Left Ventricle	heart
15	chr5:111628000-111629200	Weak transcription	Right Ventricle	heart
16	chr5:111628400-111628800	Weak transcription	Fetal Heart	heart
17	chr5:111628800-111631600	Enhancers	Fetal Heart	heart
18	chr5:111629200-111629600	Flanking Active TSS	Left Ventricle	heart
19	chr5:111629200-111629600	Flanking Active TSS	Right Ventricle	heart
20	chr5:111629200-111630200	Enhancers	Brain Hippocampus Middle	brain
21	chr5:111629400-111630000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:111629400-111630200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:111629400-111630600	Enhancers	Right Atrium	heart
24	chr5:111629600-111630400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr5:111629600-111631000	Enhancers	Left Ventricle	heart
26	chr5:111629600-111631000	Enhancers	Right Ventricle	heart
27	chr5:111630000-111630200	Enhancers	Gastric	stomach
28	chr5:111630000-111630400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:111630000-111630400	Enhancers	Brain Anterior Caudate	brain
30	chr5:111630000-111630600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:111630000-111631000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:111630400-111639600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:111631000-111632200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:111631000-111639400	Weak transcription	Left Ventricle	heart
35	chr5:111631000-111639600	Weak transcription	Right Ventricle	heart
36	chr5:111631600-111634000	Weak transcription	Fetal Heart	heart
37	chr5:111634000-111634400	ZNF genes & repeats	Fetal Heart	heart
38	chr5:111634800-111637000	Weak transcription	Aorta	Aorta
39	chr5:111635200-111638600	Weak transcription	Fetal Heart	heart
40	chr5:111635600-111651800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr5:111636400-111639800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr5:111636400-111640400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:111636800-111637000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:111636800-111637200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:111637000-111637200	Weak transcription	Lung	lung
46	chr5:111637000-111637200	ZNF genes & repeats	Pancreas	Pancrea
47	chr5:111637000-111637400	ZNF genes & repeats	Aorta	Aorta
48	chr5:111637000-111639000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:111637000-111642200	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr5:111637200-111637400	Enhancers	Lung	lung

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