Variant report

Variant	nsv1015534
Chromosome Location	chr9:607295-816742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3020)
CpG islands
(count:367)
Chromatin interactive
region (count:84)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3020 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:755679-756377	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:764021-764430	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
16	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
18	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
19	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:652937-653241	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
22	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
24	BATF	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
25	BATF	chr9:755709-756109	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
26	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
31	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
33	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
34	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
35	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
36	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
37	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
38	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
40	BRCA1	chr9:756272-756352	HepG2	liver:	n/a	n/a
41	BRCA1	chr9:763966-764464	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr9:763894-764606	HCT-116	colon:	n/a	n/a
44	CEBPB	chr9:650475-650734	HepG2	liver:	n/a	chr9:650606-650617
45	CEBPB	chr9:618414-618785	IMR90	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
46	CEBPB	chr9:761422-761787	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:799183-799446	HepG2	liver:	n/a	chr9:799301-799312
48	CEBPB	chr9:653004-653086	K562	blood:	n/a	n/a
49	CEBPB	chr9:673657-674592	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:792687-793022	Hela-S3	cervix:	n/a	chr9:792818-792829 chr9:792819-792830

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:707387-707437	BJ	skin:	n/a
2	chr9:707387-707437	BJ	skin:	n/a
3	chr9:714269-714319	ProgFib	skin:	n/a
4	chr9:705143-705193	GM12878	blood:	n/a
5	chr9:761482-761532	SKMC	muscle:	n/a
6	chr9:707410-707460	MCF10A-Er-Src	breast:	n/a
7	chr9:707166-707216	AoSMC	blood vessel:	n/a
8	chr9:707387-707437	MCF10A-Er-Src	breast:	n/a
9	chr9:707387-707437	NB4	blood:	n/a
10	chr9:707166-707216	IMR90	lung:	fetal
11	chr9:761482-761532	MCF-7	breast:	n/a
12	chr9:705143-705193	SK-N-SH_RA	brain:	n/a
13	chr9:707166-707216	ProgFib	skin:	n/a
14	chr9:707166-707216	HRE	kidney:	n/a
15	chr9:705143-705193	GM12892	blood:	n/a
16	chr9:714269-714319	SKMC	muscle:	n/a
17	chr9:705143-705193	HepG2	liver:	n/a
18	chr9:705143-705193	Hela-S3	cervix:	n/a
19	chr9:707410-707460	HNPCEpiC	eye:	n/a
20	chr9:761482-761532	BJ	skin:	n/a
21	chr9:707410-707460	GM06990	blood:	n/a
22	chr9:707166-707216	HRPEpiC	eye:	n/a
23	chr9:707410-707460	HL-60	blood:	n/a
24	chr9:707387-707437	K562	blood:	n/a
25	chr9:707387-707437	AG09319	gingival:	n/a
26	chr9:714269-714319	BJ	skin:	n/a
27	chr9:707166-707216	NH-A	brain:	n/a
28	chr9:707166-707216	HCM	heart:	n/a
29	chr9:707166-707216	GM12878	blood:	n/a
30	chr9:707387-707437	Caco-2	colon:	n/a
31	chr9:707410-707460	SAEC	small airway:	n/a
32	chr9:707166-707216	GM06990	blood:	n/a
33	chr9:707166-707216	PFSK-1	brain:	n/a
34	chr9:707410-707460	HCPEpiC	choroid plexus:	n/a
35	chr9:714269-714319	HCF	heart:	n/a
36	chr9:761482-761532	HNPCEpiC	eye:	n/a
37	chr9:705143-705193	HCF	heart:	n/a
38	chr9:707387-707437	IMR90	lung:	fetal
39	chr9:707166-707216	HCF	heart:	n/a
40	chr9:761482-761532	HUVEC	blood vessel:	n/a
41	chr9:707410-707460	A549	lung:	n/a
42	chr9:761482-761532	AG09319	gingival:	n/a
43	chr9:707410-707460	HEK293	kidney:	embryo
44	chr9:707166-707216	AG04450	lung:	fetal
45	chr9:707166-707216	HepG2	liver:	n/a
46	chr9:707166-707216	U87	brain:	n/a
47	chr9:707410-707460	BE2_C	brain:	n/a
48	chr9:707410-707460	NH-A	brain:	n/a
49	chr9:707387-707437	U87	brain:	n/a
50	chr9:705143-705193	ovcar-3	ovarian:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:763938..764768-chr9:1004823..1005723,3	MCF-7	breast:
2	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
3	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
4	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
5	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
6	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
7	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
8	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
9	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
10	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
11	chr9:682966..685572-chr9:709711..712587,2	MCF-7	breast:
12	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
13	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
14	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
15	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
16	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
17	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
18	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
19	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
20	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
21	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
22	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
23	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
24	chr9:706307..708254-chr9:737100..740465,4	MCF-7	breast:
25	chr8:128752586..128753455-chr9:706903..707668,2	NB4	blood:
26	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
27	chr9:705245..708353-chr9:743847..747461,3	MCF-7	breast:
28	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
29	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
30	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
31	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
32	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
33	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
34	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
35	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
36	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
37	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
38	chr9:730043..732840-chr9:737557..739917,2	MCF-7	breast:
39	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
40	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
41	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
42	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
43	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
44	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
45	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
46	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
47	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
48	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
49	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
50	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
2	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.1
3	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
4	lnc-C9orf66-3	chr9:674124-674379	ENSG00000227914.3
5	lnc-C9orf66-4	chr9:749336-749496	XLOC_007628
6	lnc-C9orf66-5	chr9:755232-755507	XLOC_007629
7	lnc-KANK1-1	chr9:747272-747365	NONHSAT129937
8	lnc-C9orf66-3	chr9:673478-674379	ENSG00000227914.3
9	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.1
10	lnc-KANK1-1	chr9:746431-746497	NONHSAT129937
11	lnc-C9orf66-4	chr9:749336-749509	XLOC_007628
12	lnc-KANK1-1	chr9:747412-747469	NONHSAT129937
13	lnc-C9orf66-4	chr9:761299-761551	XLOC_007628
14	lnc-C9orf66-3	chr9:677542-677628	ENSG00000227914.3
15	lnc-DMRT1-3	chr9:659986-660326	NONHSAT129934
16	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.3
17	lnc-C9orf66-3	chr9:673817-674379	ENSG00000227914.1
18	lnc-KANK1-1	chr9:748000-751056	NONHSAT129937
19	lnc-C9orf66-5	chr9:752722-752856	XLOC_007629
20	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.3

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KANK1	hsa-miR-335-5p	chr9:746085-746104
2	KANK1	hsa-miR-335-5p	chr9:746049-746071
3	KANK1	hsa-miR-124-3p	chr9:746055-746062
4	KANK1	hsa-miR-10a-5p	chr9:745092-745115
5	KANK1	hsa-miR-124-3p	chr9:746043-746062

Variant related genes	Relation type
ENSG00000227914	TF binding region
KANK1	TF binding region
ENSG00000229875	TF binding region
ENSG00000227914	CpG island
KANK1	CpG island
ENSG00000229875	CpG island
ENSG00000227914	chromatin interactions
ENSG00000108557	chromatin interactions
ENSG00000107104	chromatin interactions
SOD2	miRNA target sites
FAM123B	miRNA target sites
PPM1A	miRNA target sites

Extended variants
information (count: 11988 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:11988 , 50 per page) page: 1 2 3 4 5 6 7 ... 240

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566130968	chr9:607313-607314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140860954	chr9:607315-607316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2804307	chr9:607324-607325	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs374195210	chr9:607331-607332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575276159	chr9:607337-607338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150164353	chr9:607353-607354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111634336	chr9:607354-607355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577732000	chr9:607355-607356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540543845	chr9:607374-607375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7853384	chr9:607377-607378	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529200767	chr9:607381-607382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2804308	chr9:607382-607383	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs190439414	chr9:607383-607384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7849766	chr9:607391-607392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553484823	chr9:607400-607401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181890139	chr9:607410-607411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527830427	chr9:607420-607421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547578070	chr9:607439-607440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576402477	chr9:607440-607441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149238523	chr9:607464-607465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146965753	chr9:607473-607474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372050397	chr9:607485-607486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548730086	chr9:607531-607532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568805873	chr9:607547-607548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537559335	chr9:607553-607554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557792849	chr9:607568-607569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7873666	chr9:607632-607633	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs72689671	chr9:607648-607649	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs574018698	chr9:607655-607656	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs137974786	chr9:607682-607683	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs562763896	chr9:607684-607685	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs576353512	chr9:607702-607703	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs370242581	chr9:607732-607733	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs143998185	chr9:607737-607738	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs7850218	chr9:607738-607739	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369806854	chr9:607762-607763	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs75192804	chr9:607785-607786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs118103198	chr9:607793-607794	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs542156161	chr9:607799-607800	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs9696200	chr9:607816-607817	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568769402	chr9:607898-607899	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs537802740	chr9:607899-607900	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs9696204	chr9:607901-607902	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs72689674	chr9:607922-607923	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs147288839	chr9:607924-607925	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs541505976	chr9:607936-607937	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs148768655	chr9:607941-607942	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs202196992	chr9:607942-607943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs77798151	chr9:607943-607944	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs141602534	chr9:607952-607953	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	21272361	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:6053 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:590000-625000	Weak transcription	Aorta	Aorta
2	chr9:590200-621600	Weak transcription	Psoas Muscle	Psoas
3	chr9:592600-614400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:593000-608600	Weak transcription	Esophagus	oesophagus
5	chr9:595600-614000	Weak transcription	Right Ventricle	heart
6	chr9:596600-610800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:602000-613400	Weak transcription	A549	lung
8	chr9:603600-608400	Weak transcription	Fetal Heart	heart
9	chr9:603800-613200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr9:605800-610600	Weak transcription	Fetal Intestine Small	intestine
11	chr9:606000-607600	Weak transcription	Left Ventricle	heart
12	chr9:606000-610400	Weak transcription	Fetal Intestine Large	intestine
13	chr9:606000-628200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr9:606200-608600	Weak transcription	Brain Hippocampus Middle	brain
15	chr9:606600-609000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:606800-607400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:606800-609000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr9:606800-609000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr9:606800-609200	Enhancers	HMEC	breast
20	chr9:607000-607600	Enhancers	NHEK	skin
21	chr9:607200-607600	Enhancers	Pancreas	Pancrea
22	chr9:607200-607800	Enhancers	Placenta Amnion	Placenta Amnion
23	chr9:607400-608400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:607600-607800	Enhancers	Left Ventricle	heart
25	chr9:607600-608000	Flanking Active TSS	NHEK	skin
26	chr9:607600-608800	Weak transcription	Pancreas	Pancrea
27	chr9:607800-608600	Weak transcription	Left Ventricle	heart
28	chr9:607800-608600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr9:608000-608600	Enhancers	NHEK	skin
30	chr9:608400-609000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:608400-609000	Enhancers	Fetal Heart	heart
32	chr9:608600-608800	Enhancers	Left Ventricle	heart
33	chr9:608600-609000	Enhancers	Brain Anterior Caudate	brain
34	chr9:608600-609000	Enhancers	Brain Cingulate Gyrus	brain
35	chr9:608600-609000	Enhancers	Brain Hippocampus Middle	brain
36	chr9:608600-609000	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
37	chr9:608600-609000	Enhancers	Esophagus	oesophagus
38	chr9:608600-609000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr9:608600-609000	Enhancers	Right Atrium	heart
40	chr9:608600-609000	Bivalent Enhancer	Small Intestine	intestine
41	chr9:608600-609000	Enhancers	Spleen	Spleen
42	chr9:608600-609000	Genic enhancers	NHEK	skin
43	chr9:608800-609000	Enhancers	Brain Angular Gyrus	brain
44	chr9:608800-609000	Enhancers	Gastric	stomach
45	chr9:608800-609000	Genic enhancers	Left Ventricle	heart
46	chr9:608800-609000	Enhancers	Pancreas	Pancrea
47	chr9:609000-610400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr9:609000-610400	Weak transcription	Fetal Heart	heart
49	chr9:609000-610600	Weak transcription	Brain Hippocampus Middle	brain
50	chr9:609000-610800	Weak transcription	Brain Cingulate Gyrus	brain

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