Variant report

Variant	nsv615743
Chromosome Location	chr9:136835343-136874158
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1837)
CpG islands
(count:1405)
Chromatin interactive
region (count:108)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1837 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136859562-136859782	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:136856048-136856079	HepG2	liver:	n/a	n/a
3	BACH1	chr9:136856855-136856872	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:136857281-136858367	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:136856324-136856351	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:136858165-136858241	K562	blood:	n/a	n/a
7	BCL3	chr9:136857966-136858629	A549	lung:	n/a	chr9:136858041-136858050 chr9:136858023-136858032 chr9:136858029-136858038
8	BCL3	chr9:136857104-136857688	GM12878	blood:	n/a	chr9:136857527-136857540 chr9:136857667-136857680 chr9:136857587-136857600
9	BCLAF1	chr9:136857949-136858391	GM12878	blood:	n/a	chr9:136858041-136858050 chr9:136858023-136858032 chr9:136858029-136858038
10	BCLAF1	chr9:136857182-136857925	GM12878	blood:	n/a	chr9:136857527-136857540 chr9:136857722-136857735 chr9:136857667-136857680 chr9:136857587-136857600 chr9:136857703-136857716
11	BHLHE40	chr9:136857536-136857643	K562	blood:	n/a	n/a
12	BHLHE40	chr9:136857238-136857657	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:136869547-136869987	K562	blood:	n/a	chr9:136869715-136869728 chr9:136869957-136869973 chr9:136869906-136869915 chr9:136869716-136869725
14	BHLHE40	chr9:136858375-136858412	K562	blood:	n/a	n/a
15	BHLHE40	chr9:136859537-136859868	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:136858022-136858718	GM12878	blood:	n/a	chr9:136858292-136858308
17	BHLHE40	chr9:136857175-136857795	GM12878	blood:	n/a	chr9:136857723-136857739
18	BHLHE40	chr9:136835445-136835688	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:136856410-136856656	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:136843682-136844132	HepG2	liver:	n/a	chr9:136843822-136843838
21	BHLHE40	chr9:136869497-136870038	HepG2	liver:	n/a	chr9:136869715-136869728 chr9:136869957-136869973 chr9:136869906-136869915 chr9:136869716-136869725
22	BHLHE40	chr9:136838465-136838829	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:136859506-136859800	K562	blood:	n/a	n/a
24	BHLHE40	chr9:136869721-136869754	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:136836693-136837055	GM12878	blood:	n/a	n/a
26	BRCA1	chr9:136856472-136856482	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr9:136843712-136843912	HepG2	liver:	n/a	n/a
28	BRCA1	chr9:136837095-136837507	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr9:136859571-136859661	HepG2	liver:	n/a	n/a
30	BRCA1	chr9:136857229-136857386	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr9:136858624-136858795	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr9:136859697-136859701	GM12878	blood:	n/a	n/a
33	BRCA1	chr9:136859495-136859859	Hela-S3	cervix:	n/a	n/a
34	CCNT2	chr9:136857387-136858522	K562	blood:	n/a	chr9:136858030-136858039 chr9:136858444-136858453
35	CEBPB	chr9:136856519-136856548	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:136858552-136858776	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:136843621-136844011	HepG2	liver:	n/a	chr9:136843812-136843823 chr9:136843810-136843823 chr9:136843812-136843823 chr9:136843810-136843821
38	CEBPB	chr9:136856052-136856100	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:136843611-136844062	HepG2	liver:	n/a	chr9:136843812-136843823 chr9:136843810-136843823 chr9:136843812-136843823 chr9:136843810-136843821
40	CEBPB	chr9:136862197-136862411	HepG2	liver:	n/a	chr9:136862275-136862286
41	CEBPB	chr9:136843701-136843897	Hela-S3	cervix:	n/a	chr9:136843812-136843823 chr9:136843810-136843823 chr9:136843812-136843823 chr9:136843810-136843821
42	CEBPB	chr9:136852347-136852415	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:136856033-136856632	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:136858000-136858845	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr9:136858693-136858716	K562	blood:	n/a	n/a
46	CEBPB	chr9:136857190-136857515	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr9:136864401-136864645	IMR90	lung:	n/a	chr9:136864525-136864536
48	CEBPB	chr9:136862155-136862420	Hela-S3	cervix:	n/a	chr9:136862275-136862286
49	CEBPB	chr9:136858175-136858310	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:136859569-136859830	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136838534-136838584	Jurkat	blood:	n/a
2	chr9:136855902-136855952	HepG2	liver:	n/a
3	chr9:136838534-136838584	Jurkat	blood:	n/a
4	chr9:136855902-136855952	HepG2	liver:	n/a
5	chr9:136836252-136836302	NH-A	brain:	n/a
6	chr9:136858673-136858723	SK-N-SH_RA	brain:	n/a
7	chr9:136843224-136843274	PFSK-1	brain:	n/a
8	chr9:136857244-136857294	HEK293	kidney:	embryo
9	chr9:136858163-136858213	HEK293	kidney:	embryo
10	chr9:136873539-136873589	SK-N-MC	brain:	n/a
11	chr9:136838534-136838584	SKMC	muscle:	n/a
12	chr9:136855902-136855952	GM06990	blood:	n/a
13	chr9:136844397-136844447	HNPCEpiC	eye:	n/a
14	chr9:136844397-136844447	GM06990	blood:	n/a
15	chr9:136844397-136844447	SK-N-SH	brain:	n/a
16	chr9:136856435-136856485	HL-60	blood:	n/a
17	chr9:136858680-136858730	SK-N-MC	brain:	n/a
18	chr9:136858308-136858358	GM19239	blood:	n/a
19	chr9:136844644-136844694	SK-N-MC	brain:	n/a
20	chr9:136843224-136843274	GM06990	blood:	n/a
21	chr9:136856435-136856485	HRPEpiC	eye:	n/a
22	chr9:136873539-136873589	Hepatocyte	liver:	n/a
23	chr9:136837406-136837456	HMEC	breast:	n/a
24	chr9:136858673-136858723	MCF-7	breast:	n/a
25	chr9:136856352-136856402	T-47D	breast:	n/a
26	chr9:136858163-136858213	HNPCEpiC	eye:	n/a
27	chr9:136842323-136842373	HUVEC	blood vessel:	n/a
28	chr9:136856435-136856485	HCT-116	colon:	n/a
29	chr9:136856352-136856402	AoSMC	blood vessel:	n/a
30	chr9:136857244-136857294	SK-N-MC	brain:	n/a
31	chr9:136844397-136844447	RPTEC	kidney:	n/a
32	chr9:136843224-136843274	SAEC	small airway:	n/a
33	chr9:136873539-136873589	HAEpiC	amniotic membrane:	n/a
34	chr9:136861819-136861869	HCT-116	colon:	n/a
35	chr9:136873539-136873589	BJ	skin:	n/a
36	chr9:136860187-136860237	HEK293	kidney:	embryo
37	chr9:136843224-136843274	MCF-7	breast:	n/a
38	chr9:136855902-136855952	HRCEpiC	kidney:	n/a
39	chr9:136858308-136858358	GM12878	blood:	n/a
40	chr9:136869371-136869421	HCM	heart:	n/a
41	chr9:136844644-136844694	AG09319	gingival:	n/a
42	chr9:136856435-136856485	SK-N-MC	brain:	n/a
43	chr9:136847709-136847759	SK-N-SH	brain:	n/a
44	chr9:136858680-136858730	RPTEC	kidney:	n/a
45	chr9:136860187-136860237	Hepatocyte	liver:	n/a
46	chr9:136858163-136858213	GM06990	blood:	n/a
47	chr9:136855902-136855952	GM12892	blood:	n/a
48	chr9:136837406-136837456	GM19239	blood:	n/a
49	chr9:136842323-136842373	HCF	heart:	n/a
50	chr9:136847709-136847759	MCF10A-Er-Src	breast:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:136844757..136847399-chr9:136850001..136852495,3	MCF-7	breast:
2	chr9:136867977..136869664-chr9:136870201..136872512,2	MCF-7	breast:
3	chr9:136839997..136844319-chr9:136851053..136854251,5	MCF-7	breast:
4	chr9:136868478..136870718-chr9:136870776..136873148,2	K562	blood:
5	chr9:136866726..136869330-chr9:136873056..136875890,3	MCF-7	breast:
6	chr9:136857648..136860079-chr9:136868960..136870875,2	MCF-7	breast:
7	chr9:136600362..136604558-chr9:136857405..136860234,5	MCF-7	breast:
8	chr9:136824147..136826582-chr9:136846037..136848091,2	MCF-7	breast:
9	chr9:136855434..136861951-chr9:136862866..136866695,10	MCF-7	breast:
10	chr9:136657344..136658870-chr9:136843564..136845093,2	K562	blood:
11	chr9:136647007..136648956-chr9:136858795..136860235,12	MCF-7	breast:
12	chr9:136657819..136658763-chr9:136858806..136859951,5	MCF-7	breast:
13	chr17:41465782..41466571-chr9:136857818..136858531,2	Hela-S3	cervix:
14	chr9:136858439..136860470-chr9:136963479..136965806,2	MCF-7	breast:
15	chr9:136840615..136846826-chr9:136854892..136859021,10	MCF-7	breast:
16	chr9:136840954..136843930-chr9:136846251..136850265,3	K562	blood:
17	chr9:136834147..136836110-chr9:136837222..136840817,3	MCF-7	breast:
18	chr17:58677435..58680394-chr9:136857896..136860386,2	MCF-7	breast:
19	chr9:136830027..136831727-chr9:136833822..136836269,2	MCF-7	breast:
20	chr9:136870803..136872664-chr9:136932233..136934432,2	MCF-7	breast:
21	chr17:7387387..7388059-chr9:136856964..136857786,2	Hela-S3	cervix:
22	chr22:43010797..43011769-chr9:136856743..136857657,2	Hela-S3	cervix:
23	chr9:136819042..136820561-chr9:136859120..136860817,2	MCF-7	breast:
24	chr9:136839997..136844319-chr9:136851053..136854251,5	MCF-7	breast:
25	chr9:136608029..136608531-chr9:136858192..136859169,2	MCF-7	breast:
26	chr9:136862110..136863707-chr9:136863725..136867446,4	MCF-7	breast:
27	chr9:136835959..136838306-chr9:136857880..136859486,2	MCF-7	breast:
28	chr9:136738035..136740400-chr9:136850110..136852807,2	MCF-7	breast:
29	chr9:136372726..136374611-chr9:136854336..136856756,2	MCF-7	breast:
30	chr9:136857193..136859735-chr9:136888278..136891342,4	MCF-7	breast:
31	chr9:136873407..136875793-chr9:136883186..136885281,2	MCF-7	breast:
32	chr9:136741297..136743504-chr9:136863564..136865596,2	MCF-7	breast:
33	chr9:136859431..136860674-chr9:136964030..136964900,5	MCF-7	breast:
34	chr9:136831784..136833535-chr9:136837068..136839039,2	MCF-7	breast:
35	chr9:136739328..136742123-chr9:136841796..136845434,3	MCF-7	breast:
36	chr9:136836160..136840287-chr9:136840459..136843890,5	MCF-7	breast:
37	chr9:136841663..136844202-chr9:136856477..136858166,2	K562	blood:
38	chr9:136657888..136659088-chr9:136857891..136858693,4	MCF-7	breast:
39	chr9:136815020..136816601-chr9:136860068..136862429,2	MCF-7	breast:
40	chr9:136835900..136838442-chr9:136840312..136842040,2	K562	blood:
41	chr9:136858694..136861040-chr9:136863202..136865256,2	MCF-7	breast:
42	chr9:136821904..136824368-chr9:136852633..136855112,2	MCF-7	breast:
43	chr9:136834147..136836110-chr9:136837222..136840817,3	MCF-7	breast:
44	chr9:136646919..136648935-chr9:136858713..136860466,10	MCF-7	breast:
45	chr9:136657265..136659232-chr9:136854243..136855846,2	K562	blood:
46	chr9:123868745..123871334-chr9:136846046..136848204,2	MCF-7	breast:
47	chr9:136647156..136647722-chr9:136857760..136858312,2	MCF-7	breast:
48	chr9:136704214..136705885-chr9:136852760..136855283,2	MCF-7	breast:
49	chr9:136662303..136663068-chr9:136859673..136860648,2	MCF-7	breast:
50	chr20:48329316..48329843-chr9:136855861..136856467,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR5-7	chr9:136857728-136861324	NONHSAT135347

No data

Variant related genes	Relation type
VAV2	TF binding region
VAV2	CpG island
ENSG00000122566	chromatin interactions
ENSG00000123453	chromatin interactions
ENSG00000160293	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000169925	chromatin interactions
ENSG00000235106	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000055070	chromatin interactions
ENSG00000037637	chromatin interactions

Extended variants
information (count: 1775 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3780792	chr9:136835343-136835344	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	disease
2	rs537873816	chr9:136835383-136835384	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570680601	chr9:136835384-136835385	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144010168	chr9:136835386-136835387	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574604310	chr9:136835399-136835400	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541974058	chr9:136835404-136835405	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs57874578	chr9:136835407-136835408	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371526517	chr9:136835416-136835417	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs572257012	chr9:136835421-136835422	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183588609	chr9:136835434-136835435	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs539602538	chr9:136835473-136835474	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs188660217	chr9:136835476-136835477	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs438210	chr9:136835486-136835487	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs144883625	chr9:136835528-136835529	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs562610942	chr9:136835533-136835534	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs371148575	chr9:136835534-136835535	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs149066332	chr9:136835539-136835540	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs548719220	chr9:136835591-136835592	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs57332343	chr9:136835601-136835602	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2519140	chr9:136835615-136835616	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs2519139	chr9:136835632-136835633	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs2810542	chr9:136835660-136835661	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs2519138	chr9:136835704-136835705	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2428086	chr9:136835713-136835714	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs2492063	chr9:136835716-136835717	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115981929	chr9:136835763-136835764	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541492448	chr9:136835764-136835765	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560681230	chr9:136835829-136835830	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553878500	chr9:136835842-136835843	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572132069	chr9:136835853-136835854	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575284492	chr9:136835859-136835860	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373004073	chr9:136835860-136835861	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75068726	chr9:136835885-136835886	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35391704	chr9:136835911-136835912	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2506686	chr9:136835918-136835919	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575948157	chr9:136835925-136835926	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544162192	chr9:136835981-136835982	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562548477	chr9:136836007-136836008	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10124419	chr9:136836071-136836072	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541950823	chr9:136836083-136836084	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560667570	chr9:136836105-136836106	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527857225	chr9:136836121-136836122	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552823878	chr9:136836139-136836140	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62577870	chr9:136836146-136836147	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs532052959	chr9:136836154-136836155	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549751412	chr9:136836158-136836159	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116013704	chr9:136836172-136836173	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114345354	chr9:136836194-136836195	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553565539	chr9:136836195-136836196	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs618439	chr9:136836196-136836197	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136822600-136837000	Weak transcription	Colon Smooth Muscle	Colon
2	chr9:136822800-136836600	Weak transcription	NHDF-Ad	bronchial
3	chr9:136824400-136836800	Weak transcription	NH-A	brain
4	chr9:136824800-136835800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:136825600-136836800	Weak transcription	NHLF	lung
6	chr9:136826000-136839200	Weak transcription	Left Ventricle	heart
7	chr9:136826200-136835800	Weak transcription	Ovary	ovary
8	chr9:136826200-136835800	Weak transcription	Right Atrium	heart
9	chr9:136826800-136835600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr9:136827400-136835800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:136828000-136836600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr9:136828800-136835800	Weak transcription	HepG2	liver
13	chr9:136831800-136836200	Weak transcription	Liver	Liver
14	chr9:136832000-136840800	Enhancers	Primary B cells from cord blood	blood
15	chr9:136832400-136842400	Enhancers	Primary B cells from peripheral blood	blood
16	chr9:136832600-136843800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr9:136832800-136844200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:136833000-136836200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:136833200-136839800	Enhancers	Fetal Brain Female	brain
20	chr9:136833400-136837800	Enhancers	NHEK	skin
21	chr9:136833600-136835400	Strong transcription	Fetal Intestine Small	intestine
22	chr9:136833600-136837400	Enhancers	Fetal Stomach	stomach
23	chr9:136833600-136839600	Enhancers	Fetal Brain Male	brain
24	chr9:136833600-136839800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:136833600-136839800	Enhancers	Fetal Muscle Leg	muscle
26	chr9:136833600-136842000	Enhancers	Pancreas	Pancrea
27	chr9:136833800-136835600	Enhancers	HMEC	breast
28	chr9:136833800-136837600	Enhancers	Placenta	Placenta
29	chr9:136833800-136839600	Enhancers	Brain Germinal Matrix	brain
30	chr9:136833800-136840200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:136834000-136838800	Enhancers	GM12878-XiMat	blood
32	chr9:136834000-136840000	Enhancers	Fetal Muscle Trunk	muscle
33	chr9:136834000-136840400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr9:136834200-136835600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr9:136834200-136836000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:136834200-136837600	Enhancers	Esophagus	oesophagus
37	chr9:136834200-136840400	Enhancers	Spleen	Spleen
38	chr9:136834400-136835400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:136834400-136837400	Enhancers	Lung	lung
40	chr9:136834400-136837600	Enhancers	Placenta Amnion	Placenta Amnion
41	chr9:136834400-136838200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr9:136834600-136838600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:136834600-136839200	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr9:136834800-136835600	Enhancers	Hela-S3	cervix
45	chr9:136834800-136835800	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr9:136834800-136835800	Weak transcription	Fetal Lung	lung
47	chr9:136834800-136836000	Weak transcription	Stomach Smooth Muscle	stomach
48	chr9:136834800-136836800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr9:136835000-136835400	Weak transcription	Right Ventricle	heart
50	chr9:136835000-136836000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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