Variant report

Variant	nsv540176
Chromosome Location	chr9:98322355-98442175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:591)
CpG islands
(count:245)
Chromatin interactive
region (count:65)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:98390107-98390320	K562	blood:	n/a	n/a
2	ATF3	chr9:98357180-98357475	K562	blood:	n/a	n/a
3	BACH1	chr9:98348938-98349064	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr9:98412519-98412663	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:98379287-98379375	K562	blood:	n/a	n/a
6	BHLHE40	chr9:98340306-98340340	K562	blood:	n/a	n/a
7	BHLHE40	chr9:98391264-98391421	K562	blood:	n/a	n/a
8	BHLHE40	chr9:98339250-98339436	K562	blood:	n/a	n/a
9	CEBPB	chr9:98389325-98389455	Hela-S3	cervix:	n/a	chr9:98389387-98389400
10	CEBPB	chr9:98355242-98355585	IMR90	lung:	n/a	chr9:98355411-98355422
11	CEBPB	chr9:98357189-98357488	K562	blood:	n/a	n/a
12	CEBPB	chr9:98348174-98348422	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:98341216-98341416	IMR90	lung:	n/a	chr9:98341348-98341359
14	CEBPB	chr9:98404947-98405107	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:98406116-98406255	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:98411949-98412187	HepG2	liver:	n/a	chr9:98412048-98412059
17	CEBPB	chr9:98341224-98341447	A549	lung:	n/a	chr9:98341348-98341359
18	CEBPB	chr9:98413740-98413929	HepG2	liver:	n/a	chr9:98413832-98413843
19	CEBPB	chr9:98337324-98337494	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:98343896-98344551	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr9:98390069-98390396	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:98357179-98357447	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:98348181-98348412	A549	lung:	n/a	n/a
24	CEBPB	chr9:98341266-98341457	HepG2	liver:	n/a	chr9:98341348-98341359
25	CEBPB	chr9:98357200-98357461	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:98355243-98355579	HepG2	liver:	n/a	chr9:98355411-98355422
27	CEBPB	chr9:98369207-98369377	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:98355191-98355613	K562	blood:	n/a	chr9:98355411-98355422
29	CEBPB	chr9:98355250-98355547	Hela-S3	cervix:	n/a	chr9:98355411-98355422
30	CEBPB	chr9:98355194-98355548	K562	blood:	n/a	chr9:98355411-98355422
31	CEBPB	chr9:98355398-98355572	H1-hESC	embryonic stem cell:	n/a	chr9:98355411-98355422
32	CEBPB	chr9:98355235-98355543	K562	blood:	n/a	chr9:98355411-98355422
33	CEBPB	chr9:98437498-98437727	HepG2	liver:	n/a	chr9:98437592-98437605 chr9:98437592-98437603 chr9:98437594-98437603
34	CEBPB	chr9:98355244-98355586	A549	lung:	n/a	chr9:98355411-98355422
35	CEBPB	chr9:98389338-98389494	H1-hESC	embryonic stem cell:	n/a	chr9:98389387-98389400
36	CEBPB	chr9:98357166-98357410	K562	blood:	n/a	n/a
37	CEBPB	chr9:98411949-98412188	Hela-S3	cervix:	n/a	chr9:98412048-98412059
38	CEBPB	chr9:98408469-98408540	K562	blood:	n/a	n/a
39	CEBPB	chr9:98348263-98348343	IMR90	lung:	n/a	n/a
40	CEBPB	chr9:98348266-98348357	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr9:98357257-98357397	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:98408366-98408572	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:98389380-98389409	K562	blood:	n/a	chr9:98389387-98389400
44	CEBPD	chr9:98391900-98392218	K562	blood:	n/a	n/a
45	CHD2	chr9:98343932-98344276	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTBP2	chr9:98343827-98344512	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:98380620-98380770	K562	blood:	n/a	n/a
48	CTCF	chr9:98336446-98336832	GM12878	blood:	n/a	n/a
49	CTCF	chr9:98336829-98336945	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:98380580-98380730	WERI-Rb-1	eye:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98389082-98389132	HMEC	breast:	n/a
2	chr9:98389082-98389132	HMEC	breast:	n/a
3	chr9:98368382-98368432	A549	lung:	n/a
4	chr9:98389082-98389132	HNPCEpiC	eye:	n/a
5	chr9:98343728-98343778	T-47D	breast:	n/a
6	chr9:98343728-98343778	AG09309	skin:	n/a
7	chr9:98343728-98343778	SK-N-MC	brain:	n/a
8	chr9:98368382-98368432	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:98389082-98389132	HRPEpiC	eye:	n/a
10	chr9:98368382-98368432	AoSMC	blood vessel:	n/a
11	chr9:98343728-98343778	ECC-1	luminal epithelium:	n/a
12	chr9:98343728-98343778	HL-60	blood:	n/a
13	chr9:98389082-98389132	U87	brain:	n/a
14	chr9:98335074-98335124	PFSK-1	brain:	n/a
15	chr9:98343728-98343778	H1-hESC	embryonic stem cell:	embryo
16	chr9:98368382-98368432	HCF	heart:	n/a
17	chr9:98343728-98343778	K562	blood:	n/a
18	chr9:98389082-98389132	Hepatocyte	liver:	n/a
19	chr9:98368382-98368432	U87	brain:	n/a
20	chr9:98335074-98335124	PrEC	prostate:	n/a
21	chr9:98389082-98389132	AG04450	lung:	fetal
22	chr9:98389082-98389132	BJ	skin:	n/a
23	chr9:98335074-98335124	T-47D	breast:	n/a
24	chr9:98343728-98343778	NT2-D1	testis:	n/a
25	chr9:98343728-98343778	HRCEpiC	kidney:	n/a
26	chr9:98335074-98335124	MCF10A-Er-Src	breast:	n/a
27	chr9:98335074-98335124	HRCEpiC	kidney:	n/a
28	chr9:98368382-98368432	AG10803	skin:	n/a
29	chr9:98343728-98343778	MCF10A-Er-Src	breast:	n/a
30	chr9:98389082-98389132	T-47D	breast:	n/a
31	chr9:98389082-98389132	CMK	blood:	n/a
32	chr9:98335074-98335124	HRE	kidney:	n/a
33	chr9:98389082-98389132	AG04449	skin:	fetal
34	chr9:98389082-98389132	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:98389082-98389132	IMR90	lung:	fetal
36	chr9:98389082-98389132	Jurkat	blood:	n/a
37	chr9:98343728-98343778	HCPEpiC	choroid plexus:	n/a
38	chr9:98368382-98368432	PrEC	prostate:	n/a
39	chr9:98343728-98343778	NHDF-neo	bronchial:	n/a
40	chr9:98389082-98389132	NH-A	brain:	n/a
41	chr9:98335074-98335124	HCPEpiC	choroid plexus:	n/a
42	chr9:98368382-98368432	GM06990	blood:	n/a
43	chr9:98335074-98335124	HEEpiC	esophagus:	n/a
44	chr9:98389082-98389132	HCM	heart:	n/a
45	chr9:98343728-98343778	BE2_C	brain:	n/a
46	chr9:98389082-98389132	PFSK-1	brain:	n/a
47	chr9:98335074-98335124	NHBE	bronchial:	n/a
48	chr9:98389082-98389132	NB4	blood:	n/a
49	chr9:98343728-98343778	HMEC	breast:	n/a
50	chr9:98343728-98343778	AG04449	skin:	fetal

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:98405903..98408685-chr9:98410741..98413135,2	MCF-7	breast:
2	chr9:98272232..98274861-chr9:98331837..98334312,2	MCF-7	breast:
3	chr9:98307185..98309730-chr9:98321412..98323508,2	K562	blood:
4	chr9:98401343..98404443-chr9:98406954..98408730,3	MCF-7	breast:
5	chr11:62607631..62609200-chr9:98431711..98434711,4	K562	blood:
6	chr9:98361951..98364526-chr9:98367757..98370013,2	K562	blood:
7	chr3:73158468..73160028-chr9:98433191..98434711,2	K562	blood:
8	chr17:41464316..41464827-chr9:98433191..98433691,2	HCT-116	colon:
9	chr9:98392594..98394713-chr9:98395730..98397379,2	MCF-7	breast:
10	chr9:98393478..98395133-chr9:98395961..98397828,2	MCF-7	breast:
11	chr17:41465183..41465862-chr9:98433191..98433691,2	HCT-116	colon:
12	chr11:62608622..62609147-chr9:98433191..98433711,2	Hela-S3	cervix:
13	chr3:73160105..73160612-chr9:98433211..98433711,3	HCT-116	colon:
14	chr9:98340396..98343359-chr9:98347177..98349920,2	MCF-7	breast:
15	chr9:98323087..98325091-chr9:98326956..98328604,2	K562	blood:
16	chr9:98398821..98400681-chr9:98404972..98407509,2	K562	blood:
17	chr9:98246647..98248663-chr9:98399249..98402157,2	K562	blood:
18	chr9:98404205..98406379-chr9:98407605..98409471,2	K562	blood:
19	chr3:73159958..73161460-chr9:98422389..98425369,2	MCF-7	breast:
20	chr17:41380435..41383382-chr9:98431711..98434691,2	K562	blood:
21	chr9:98388922..98390483-chr9:98392271..98394990,2	MCF-7	breast:
22	chr9:98271289..98274209-chr9:98357697..98360375,2	MCF-7	breast:
23	chr11:62607642..62609218-chr9:98433191..98434711,3	MCF-7	breast:
24	chr9:98388922..98390483-chr9:98392271..98394990,2	MCF-7	breast:
25	chr9:98398076..98400257-chr9:98405336..98408000,2	MCF-7	breast:
26	chr17:41465183..41466775-chr9:98422369..98423869,2	MCF-7	breast:
27	chr17:41398364..41402158-chr9:98431691..98434711,6	K562	blood:
28	chr9:98404205..98406379-chr9:98407605..98409471,2	K562	blood:
29	chr9:98394128..98397071-chr9:98405043..98407151,2	MCF-7	breast:
30	chr9:98379846..98381377-chr9:99391603..99393472,2	MCF-7	breast:
31	chr9:98349544..98353253-chr9:98355727..98357613,4	K562	blood:
32	chr9:98398821..98400681-chr9:98404972..98407509,2	K562	blood:
33	chr9:98421286..98423428-chr9:98429495..98431673,2	MCF-7	breast:
34	chr9:98394128..98397071-chr9:98405043..98407151,2	MCF-7	breast:
35	chr11:62608635..62609155-chr9:98433191..98433711,4	HCT-116	colon:
36	chr9:98335123..98337480-chr9:98341108..98343369,3	MCF-7	breast:
37	chr3:73160048..73161620-chr9:98433191..98434691,2	K562	blood:
38	chr9:98340396..98343359-chr9:98347177..98349920,2	MCF-7	breast:
39	chr9:98358248..98359926-chr9:98364098..98366216,2	K562	blood:
40	chr10:103124109..103124632-chr9:98433191..98433711,2	HCT-116	colon:
41	chr9:98399194..98401092-chr9:98636282..98638706,2	MCF-7	breast:
42	chr9:98103822..98104598-chr9:98336133..98336924,2	MCF-7	breast:
43	chr17:41398401..41400225-chr9:98431711..98433211,2	MCF-7	breast:
44	chr3:73160091..73160603-chr9:98433196..98433711,2	Hela-S3	cervix:
45	chr9:98376305..98377909-chr9:98638034..98639595,2	MCF-7	breast:
46	chr9:98401343..98404443-chr9:98406954..98408730,3	MCF-7	breast:
47	chr11:62607637..62609142-chr9:98433211..98434711,2	K562	blood:
48	chr9:98360898..98362418-chr9:98636768..98638304,2	MCF-7	breast:
49	chr9:98365907..98368696-chr9:98386758..98389009,2	K562	blood:
50	chr9:98349544..98353253-chr9:98355727..98357613,4	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf102-9	chr9:98415194-98415548	NONHSAT133387
2	lnc-C9orf102-5	chr9:98412444-98412523	ENSG00000228142.2
3	lnc-PTCH1-2	chr9:98368504-98368568	XLOC_007785
4	lnc-PTCH1-2	chr9:98364253-98364441	XLOC_007785
5	lnc-PTCH1-2	chr9:98361827-98361967	XLOC_007785
6	lnc-C9orf102-5	chr9:98412436-98412523	ENSG00000228142.2

No data

Variant related genes	Relation type
ENSG00000229345	TF binding region
ENSG00000228142	TF binding region
ENSG00000227358	TF binding region
ENSG00000229345	CpG island
ENSG00000228142	CpG island
ENSG00000227358	CpG island
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000229345	chromatin interactions
ENSG00000228142	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000182150	chromatin interactions
ENSG00000175611	chromatin interactions

Extended variants
information (count: 4526 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4526 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546760075	chr9:98322364-98322365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536604126	chr9:98322397-98322398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138962065	chr9:98322404-98322405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187235476	chr9:98322405-98322406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149397163	chr9:98322454-98322455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559233953	chr9:98322498-98322499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573793790	chr9:98322544-98322545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114654214	chr9:98322617-98322618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541688788	chr9:98322644-98322645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs55701736	chr9:98322658-98322659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs66917126	chr9:98322715-98322716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs72754333	chr9:98322751-98322752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs374214031	chr9:98322761-98322762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144795734	chr9:98322806-98322807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563157821	chr9:98322821-98322822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530554942	chr9:98322822-98322823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138274725	chr9:98322831-98322832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116352738	chr9:98322852-98322853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74457780	chr9:98322864-98322865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142852359	chr9:98323000-98323001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565798873	chr9:98323033-98323034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531514108	chr9:98323065-98323066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372584484	chr9:98323121-98323122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376032398	chr9:98323128-98323129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199963986	chr9:98323142-98323143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs33986945	chr9:98323164-98323165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536365618	chr9:98323268-98323269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114489410	chr9:98323288-98323289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369217224	chr9:98323303-98323304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28424156	chr9:98323333-98323334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563844573	chr9:98323345-98323346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531272806	chr9:98323349-98323350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559288551	chr9:98323357-98323358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577613211	chr9:98323387-98323388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541596324	chr9:98323397-98323398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72754336	chr9:98323401-98323402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574554721	chr9:98323498-98323499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1464035	chr9:98323507-98323508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541538091	chr9:98323525-98323526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563433015	chr9:98323594-98323595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561016548	chr9:98323595-98323596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566560435	chr9:98323605-98323606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545830702	chr9:98323677-98323678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373521918	chr9:98323734-98323735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146105397	chr9:98323792-98323793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528381718	chr9:98323794-98323795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192160403	chr9:98323808-98323809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs59000482	chr9:98323813-98323814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397969742	chr9:98323817-98323818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561569596	chr9:98323866-98323867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98319600-98330000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:98319800-98324400	Weak transcription	Gastric	stomach
3	chr9:98319800-98329800	Weak transcription	Spleen	Spleen
4	chr9:98319800-98330000	Weak transcription	Fetal Kidney	kidney
5	chr9:98324000-98324400	Enhancers	Stomach Mucosa	stomach
6	chr9:98324400-98324600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr9:98324400-98324800	Enhancers	Gastric	stomach
8	chr9:98324800-98329800	Weak transcription	Gastric	stomach
9	chr9:98327000-98327400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:98327000-98327600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:98327200-98329600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr9:98327400-98329800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:98327600-98327800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:98327600-98327800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr9:98327600-98329200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:98328000-98329400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:98329200-98329600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr9:98329200-98330200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:98329200-98330200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr9:98329200-98330200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:98329200-98330400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:98329400-98330000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:98329600-98329800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:98329600-98329800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr9:98329600-98330000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr9:98329600-98330000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:98329600-98330000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr9:98329600-98330200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr9:98329600-98330200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:98329600-98332200	Weak transcription	Fetal Lung	lung
31	chr9:98329600-98332600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr9:98329800-98330000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:98329800-98330200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
34	chr9:98329800-98330200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr9:98329800-98330200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr9:98329800-98330200	Enhancers	Gastric	stomach
37	chr9:98329800-98330800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr9:98329800-98330800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
39	chr9:98329800-98331000	ZNF genes & repeats	Spleen	Spleen
40	chr9:98330000-98330200	Bivalent Enhancer	Fetal Brain Male	brain
41	chr9:98330000-98330400	ZNF genes & repeats	Fetal Kidney	kidney
42	chr9:98330000-98330600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr9:98330000-98330800	ZNF genes & repeats	Pancreas	Pancrea
44	chr9:98330000-98331000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr9:98330000-98331000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:98330000-98332200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr9:98330000-98332200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr9:98330200-98332200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr9:98330200-98332200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:98330200-98335000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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