Variant report

Variant	nsv1031342
Chromosome Location	chr9:525752-814210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3778)
CpG islands
(count:427)
Chromatin interactive
region (count:104)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3778 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
7	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:764021-764430	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:755679-756377	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
18	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
19	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
20	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
21	BACH1	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
22	BACH1	chr9:652937-653241	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr9:755709-756109	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
28	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
29	BATF	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
30	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
35	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
36	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
37	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
38	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
40	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
44	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
45	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
46	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
47	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
48	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
49	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr9:756272-756352	HepG2	liver:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:707410-707460	HRE	kidney:	n/a
2	chr9:707387-707437	HCM	heart:	n/a
3	chr9:707166-707216	HL-60	blood:	n/a
4	chr9:707410-707460	AG09309	skin:	n/a
5	chr9:761482-761532	HCPEpiC	choroid plexus:	n/a
6	chr9:574312-574362	HRPEpiC	eye:	n/a
7	chr9:707166-707216	ovcar-3	ovarian:	n/a
8	chr9:714269-714319	GM12891	blood:	n/a
9	chr9:705143-705193	HepG2	liver:	n/a
10	chr9:707410-707460	SK-N-SH	brain:	n/a
11	chr9:761482-761532	HCT-116	colon:	n/a
12	chr9:714269-714319	HCF	heart:	n/a
13	chr9:761482-761532	HNPCEpiC	eye:	n/a
14	chr9:705143-705193	HUVEC	blood vessel:	n/a
15	chr9:707410-707460	BE2_C	brain:	n/a
16	chr9:574312-574362	GM12892	blood:	n/a
17	chr9:714269-714319	AG04450	lung:	fetal
18	chr9:707166-707216	BE2_C	brain:	n/a
19	chr9:707166-707216	GM06990	blood:	n/a
20	chr9:574312-574362	AG04449	skin:	fetal
21	chr9:705143-705193	K562	blood:	n/a
22	chr9:574312-574362	HCT-116	colon:	n/a
23	chr9:707387-707437	BJ	skin:	n/a
24	chr9:707410-707460	MCF-7	breast:	n/a
25	chr9:707387-707437	GM19239	blood:	n/a
26	chr9:714269-714319	ECC-1	luminal epithelium:	n/a
27	chr9:707166-707216	NH-A	brain:	n/a
28	chr9:761482-761532	IMR90	lung:	fetal
29	chr9:574312-574362	Jurkat	blood:	n/a
30	chr9:705143-705193	PANC-1	pancreas:	n/a
31	chr9:707387-707437	GM12891	blood:	n/a
32	chr9:707410-707460	K562	blood:	n/a
33	chr9:707166-707216	GM12891	blood:	n/a
34	chr9:574312-574362	GM06990	blood:	n/a
35	chr9:705143-705193	A549	lung:	n/a
36	chr9:707387-707437	HCF	heart:	n/a
37	chr9:707166-707216	ECC-1	luminal epithelium:	n/a
38	chr9:761482-761532	HEEpiC	esophagus:	n/a
39	chr9:574312-574362	Caco-2	colon:	n/a
40	chr9:761482-761532	HMEC	breast:	n/a
41	chr9:714269-714319	ProgFib	skin:	n/a
42	chr9:707166-707216	Hela-S3	cervix:	n/a
43	chr9:761482-761532	Caco-2	colon:	n/a
44	chr9:707410-707460	RPTEC	kidney:	n/a
45	chr9:707166-707216	AG09319	gingival:	n/a
46	chr9:714269-714319	GM12892	blood:	n/a
47	chr9:705143-705193	GM12892	blood:	n/a
48	chr9:707166-707216	HMEC	breast:	n/a
49	chr9:707387-707437	NB4	blood:	n/a
50	chr9:574312-574362	SK-N-SH	brain:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
2	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
3	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
4	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
5	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
6	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
7	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
8	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
9	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
10	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
11	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
12	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
13	chr9:469326..471004-chr9:547085..549851,2	MCF-7	breast:
14	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
15	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
16	chr17:17584235..17586582-chr9:741151..743803,2	MCF-7	breast:
17	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
18	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
19	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
20	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
21	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
22	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
23	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
24	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
25	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
26	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
27	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
28	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
29	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
30	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
31	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
32	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
33	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
34	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
35	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
36	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
37	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
38	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
39	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
40	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
41	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
42	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
43	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
44	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
45	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
46	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
47	chr9:385566..386417-chr9:764222..764740,2	MCF-7	breast:
48	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
49	chr9:682966..685572-chr9:709711..712587,2	MCF-7	breast:
50	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-5	chr9:752722-752856	XLOC_007629
2	lnc-C9orf66-4	chr9:749336-749509	XLOC_007628
3	lnc-DMRT1-3	chr9:659986-660326	NONHSAT129934
4	lnc-C9orf66-3	chr9:677542-677628	ENSG00000227914.3
5	lnc-DOCK8-2	chr9:549107-549531	ENSG00000226403.1
6	lnc-KANK1-1	chr9:747272-747365	NONHSAT129937
7	lnc-C9orf66-3	chr9:673478-674379	ENSG00000227914.3
8	lnc-DOCK8-2	chr9:547318-547341	ENSG00000226403.1
9	lnc-KANK1-1	chr9:747412-747469	NONHSAT129937
10	lnc-DOCK8-2	chr9:549190-549531	ENSG00000226403.1
11	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
12	lnc-DOCK8-2	chr9:549107-549525	NONHSAT129931
13	lnc-C9orf66-3	chr9:673817-674379	ENSG00000227914.1
14	lnc-KANK1-1	chr9:746431-746497	NONHSAT129937
15	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.1
16	lnc-KANK1-1	chr9:748000-751056	NONHSAT129937
17	lnc-DOCK8-2	chr9:547038-547341	NONHSAT129931
18	lnc-C9orf66-3	chr9:674124-674379	ENSG00000227914.3
19	lnc-C9orf66-4	chr9:761299-761551	XLOC_007628
20	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.1
21	lnc-DOCK8-2	chr9:547317-547341	ENSG00000226403.1
22	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.3
23	lnc-C9orf66-5	chr9:755232-755507	XLOC_007629
24	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.3
25	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
26	lnc-C9orf66-4	chr9:749336-749496	XLOC_007628

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-124-3p	chr9:746055-746062
3	KANK1	hsa-miR-10a-5p	chr9:745092-745115
4	KANK1	hsa-miR-124-3p	chr9:746043-746062
5	KANK1	hsa-miR-335-5p	chr9:746049-746071

Variant related genes	Relation type
ENSG00000226403	TF binding region
RNU6-1327P	TF binding region
ENSG00000227914	TF binding region
KANK1	TF binding region
ENSG00000229875	TF binding region
ENSG00000226403	CpG island
RNU6-1327P	CpG island
ENSG00000227914	CpG island
KANK1	CpG island
ENSG00000229875	CpG island
ENSG00000108557	chromatin interactions
ENSG00000107104	chromatin interactions
ENSG00000227914	chromatin interactions
ENSG00000227155	chromatin interactions
SOD2	miRNA target sites
PPM1A	miRNA target sites
FAM123B	miRNA target sites

Extended variants
information (count: 16708 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:16708 , 50 per page) page: 1 2 3 4 5 6 7 ... 335

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184486275	chr9:525775-525776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34841646	chr9:525806-525807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7856134	chr9:525814-525815	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376460836	chr9:525848-525849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373230422	chr9:525855-525856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373442762	chr9:525871-525872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200016480	chr9:525878-525879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75639713	chr9:525881-525882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147857042	chr9:525894-525895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564189498	chr9:525902-525903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7856262	chr9:525903-525904	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140369727	chr9:525913-525914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74373422	chr9:525942-525943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186489746	chr9:525950-525951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555814908	chr9:525979-525980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528157273	chr9:525988-525989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548229682	chr9:526006-526007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4742067	chr9:526009-526010	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs72705678	chr9:526033-526034	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs550247313	chr9:526046-526047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551985980	chr9:526058-526059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571828350	chr9:526067-526068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528037875	chr9:526074-526075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546182638	chr9:526105-526106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566088333	chr9:526121-526122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72705680	chr9:526163-526164	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs541388797	chr9:526164-526165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376188561	chr9:526212-526213	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555015282	chr9:526219-526220	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568626277	chr9:526235-526236	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377293579	chr9:526240-526241	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537627986	chr9:526258-526259	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557959057	chr9:526273-526274	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577856152	chr9:526278-526279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570307361	chr9:526355-526356	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540561274	chr9:526369-526370	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554111570	chr9:526374-526375	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370730076	chr9:526384-526385	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574055026	chr9:526392-526393	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150301146	chr9:526394-526395	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376344321	chr9:526401-526402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562957229	chr9:526438-526439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72705681	chr9:526446-526447	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2022173	chr9:526455-526456	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565517156	chr9:526479-526480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144871253	chr9:526488-526489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547635144	chr9:526566-526567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192563600	chr9:526574-526575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544124772	chr9:526607-526608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528823401	chr9:526620-526621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	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-syndromic sensorineural hearing loss	21293372	CNVD
Non-small cell lung cancer	16651412	CNVD
Cancer	21272361	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:7640 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:507000-532600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:514000-532200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr9:518800-528800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:518800-529400	Weak transcription	NHEK	skin
5	chr9:518800-529600	Weak transcription	HMEC	breast
6	chr9:519400-527000	Weak transcription	Fetal Intestine Large	intestine
7	chr9:519600-528800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:520600-535000	Weak transcription	Gastric	stomach
9	chr9:521400-533000	Weak transcription	Small Intestine	intestine
10	chr9:522800-527000	Weak transcription	A549	lung
11	chr9:522800-532600	Weak transcription	Fetal Kidney	kidney
12	chr9:523000-527000	Weak transcription	Psoas Muscle	Psoas
13	chr9:523000-530800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:523200-531200	Weak transcription	Brain Substantia Nigra	brain
15	chr9:523200-532800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr9:523600-530600	Weak transcription	Fetal Muscle Leg	muscle
17	chr9:523800-530600	Weak transcription	Left Ventricle	heart
18	chr9:523800-530800	Weak transcription	Right Atrium	heart
19	chr9:523800-533600	Weak transcription	Esophagus	oesophagus
20	chr9:523800-535000	Weak transcription	Lung	lung
21	chr9:524200-531200	Weak transcription	Right Ventricle	heart
22	chr9:524600-531800	Weak transcription	Fetal Lung	lung
23	chr9:524800-526200	Weak transcription	Pancreas	Pancrea
24	chr9:524800-527400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr9:524800-529600	Weak transcription	Fetal Heart	heart
26	chr9:524800-530600	Weak transcription	Brain Hippocampus Middle	brain
27	chr9:524800-530800	Weak transcription	Stomach Smooth Muscle	stomach
28	chr9:524800-531200	Weak transcription	Aorta	Aorta
29	chr9:524800-531200	Weak transcription	Brain Anterior Caudate	brain
30	chr9:525400-526400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr9:525400-526400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:525400-526800	Strong transcription	Fetal Intestine Small	intestine
33	chr9:525400-532400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr9:526200-526400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:526200-526400	Enhancers	Pancreas	Pancrea
36	chr9:526400-527000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr9:526400-527000	Weak transcription	Pancreas	Pancrea
38	chr9:526400-528600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr9:526400-535000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:526800-528600	Weak transcription	Fetal Intestine Small	intestine
41	chr9:527000-527200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr9:527000-527400	Enhancers	Fetal Intestine Large	intestine
43	chr9:527000-527400	Enhancers	A549	lung
44	chr9:527000-527600	Enhancers	Pancreas	Pancrea
45	chr9:527000-527600	Enhancers	Psoas Muscle	Psoas
46	chr9:527200-529600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:527400-527600	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr9:527400-529600	Weak transcription	A549	lung
49	chr9:527400-532400	Weak transcription	Fetal Intestine Large	intestine
50	chr9:527600-530800	Weak transcription	Pancreas	Pancrea

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