Variant report

Variant	nsv1033964
Chromosome Location	chr9:525037-816742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3781)
CpG islands
(count:427)
Chromatin interactive
region (count:104)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3781 , 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	chr9:710020-710338	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:764021-764430	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
10	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
18	ARID3A	chr9:755679-756377	HepG2	liver:	n/a	n/a
19	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
20	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
21	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr9:652937-653241	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	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
27	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
28	BATF	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
29	BATF	chr9:755709-756109	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
30	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
35	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
36	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
37	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
38	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
40	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
43	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
44	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
45	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
46	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
47	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
49	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr9:763966-764464	H1-hESC	embryonic stem cell:	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	chr9:714269-714319	NT2-D1	testis:	n/a
2	chr9:707410-707460	HCM	heart:	n/a
3	chr9:707410-707460	AoSMC	blood vessel:	n/a
4	chr9:574312-574362	HL-60	blood:	n/a
5	chr9:761482-761532	HL-60	blood:	n/a
6	chr9:707387-707437	ProgFib	skin:	n/a
7	chr9:705143-705193	GM19239	blood:	n/a
8	chr9:707387-707437	NB4	blood:	n/a
9	chr9:707387-707437	CMK	blood:	n/a
10	chr9:705143-705193	MCF-7	breast:	n/a
11	chr9:714269-714319	NHDF-neo	bronchial:	n/a
12	chr9:707166-707216	BJ	skin:	n/a
13	chr9:707387-707437	HAEpiC	amniotic membrane:	n/a
14	chr9:574312-574362	AG09309	skin:	n/a
15	chr9:705143-705193	SKMC	muscle:	n/a
16	chr9:574312-574362	GM12892	blood:	n/a
17	chr9:707166-707216	HEK293	kidney:	embryo
18	chr9:707410-707460	PFSK-1	brain:	n/a
19	chr9:714269-714319	GM06990	blood:	n/a
20	chr9:574312-574362	SK-N-MC	brain:	n/a
21	chr9:761482-761532	SAEC	small airway:	n/a
22	chr9:574312-574362	MCF-7	breast:	n/a
23	chr9:574312-574362	HNPCEpiC	eye:	n/a
24	chr9:707387-707437	HIPEpiC	eye:	n/a
25	chr9:761482-761532	NH-A	brain:	n/a
26	chr9:705143-705193	HepG2	liver:	n/a
27	chr9:714269-714319	GM12892	blood:	n/a
28	chr9:707410-707460	Caco-2	colon:	n/a
29	chr9:707410-707460	AG10803	skin:	n/a
30	chr9:574312-574362	HRCEpiC	kidney:	n/a
31	chr9:714269-714319	HRPEpiC	eye:	n/a
32	chr9:761482-761532	AG04449	skin:	fetal
33	chr9:761482-761532	HRE	kidney:	n/a
34	chr9:707166-707216	PFSK-1	brain:	n/a
35	chr9:714269-714319	AG04450	lung:	fetal
36	chr9:707387-707437	HRCEpiC	kidney:	n/a
37	chr9:714269-714319	SK-N-SH_RA	brain:	n/a
38	chr9:707166-707216	RPTEC	kidney:	n/a
39	chr9:705143-705193	AG10803	skin:	n/a
40	chr9:707166-707216	CMK	blood:	n/a
41	chr9:574312-574362	GM06990	blood:	n/a
42	chr9:714269-714319	ProgFib	skin:	n/a
43	chr9:707410-707460	GM19239	blood:	n/a
44	chr9:574312-574362	AG04449	skin:	fetal
45	chr9:707410-707460	HMEC	breast:	n/a
46	chr9:707410-707460	ProgFib	skin:	n/a
47	chr9:707387-707437	IMR90	lung:	fetal
48	chr9:714269-714319	HCM	heart:	n/a
49	chr9:714269-714319	SK-N-MC	brain:	n/a
50	chr9:714269-714319	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
2	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
3	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
4	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
5	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
6	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
7	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
8	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
9	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
10	chr9:706377..708156-chr9:805249..808005,2	MCF-7	breast:
11	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
12	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
13	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
14	chr9:385566..386417-chr9:764222..764740,2	MCF-7	breast:
15	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
16	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
17	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
18	chr9:682966..685572-chr9:709711..712587,2	MCF-7	breast:
19	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
20	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
21	chr9:704209..707068-chr9:719899..721523,2	MCF-7	breast:
22	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
23	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
24	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
25	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
26	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
27	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
28	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
29	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
30	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
31	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
32	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
33	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
34	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
35	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
36	chr17:17584235..17586582-chr9:741151..743803,2	MCF-7	breast:
37	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
38	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
39	chr9:730043..732840-chr9:737557..739917,2	MCF-7	breast:
40	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
41	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
42	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
43	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
44	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
45	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
46	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
47	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
48	chr16:1239384..1239884-chr9:736833..737597,2	MCF-7	breast:
49	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
50	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:

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

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

No data

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

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

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
ENSG00000107104	chromatin interactions
ENSG00000227914	chromatin interactions
ENSG00000108557	chromatin interactions
ENSG00000227155	chromatin interactions
FAM123B	miRNA target sites
PPM1A	miRNA target sites
SOD2	miRNA target sites

Extended variants
information (count: 16741 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:16741 , 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	rs569549023	chr9:525068-525069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188419674	chr9:525071-525072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7027273	chr9:525080-525081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558438048	chr9:525103-525104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576718530	chr9:525183-525184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144220298	chr9:525212-525213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552760126	chr9:525234-525235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4740806	chr9:525243-525244	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529558005	chr9:525247-525248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572638287	chr9:525259-525260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541604836	chr9:525260-525261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561599070	chr9:525288-525289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575177781	chr9:525305-525306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544134363	chr9:525321-525322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369557043	chr9:525351-525352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143010173	chr9:525360-525361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35296364	chr9:525384-525385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564406292	chr9:525393-525394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6476942	chr9:525423-525424	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs6476943	chr9:525434-525435	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs142305609	chr9:525451-525452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377403096	chr9:525456-525457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529435682	chr9:525483-525484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549594993	chr9:525529-525530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147616244	chr9:525532-525533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538444799	chr9:525607-525608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551760756	chr9:525611-525612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571925428	chr9:525626-525627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539049241	chr9:525662-525663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192691659	chr9:525672-525673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143719624	chr9:525679-525680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35647518	chr9:525729-525730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144389561	chr9:525736-525737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184486275	chr9:525775-525776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34841646	chr9:525806-525807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7856134	chr9:525814-525815	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376460836	chr9:525848-525849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373230422	chr9:525855-525856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373442762	chr9:525871-525872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200016480	chr9:525878-525879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75639713	chr9:525881-525882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147857042	chr9:525894-525895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564189498	chr9:525902-525903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7856262	chr9:525903-525904	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs140369727	chr9:525913-525914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74373422	chr9:525942-525943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186489746	chr9:525950-525951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555814908	chr9:525979-525980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528157273	chr9:525988-525989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548229682	chr9:526006-526007	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:7645 , 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	chr9:519000-525400	Weak transcription	Fetal Intestine Small	intestine
7	chr9:519400-527000	Weak transcription	Fetal Intestine Large	intestine
8	chr9:519600-528800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:520600-535000	Weak transcription	Gastric	stomach
10	chr9:521400-533000	Weak transcription	Small Intestine	intestine
11	chr9:522400-525400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:522400-525400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr9:522800-527000	Weak transcription	A549	lung
14	chr9:522800-532600	Weak transcription	Fetal Kidney	kidney
15	chr9:523000-527000	Weak transcription	Psoas Muscle	Psoas
16	chr9:523000-530800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:523200-531200	Weak transcription	Brain Substantia Nigra	brain
18	chr9:523200-532800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:523600-530600	Weak transcription	Fetal Muscle Leg	muscle
20	chr9:523800-530600	Weak transcription	Left Ventricle	heart
21	chr9:523800-530800	Weak transcription	Right Atrium	heart
22	chr9:523800-533600	Weak transcription	Esophagus	oesophagus
23	chr9:523800-535000	Weak transcription	Lung	lung
24	chr9:524000-525400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr9:524200-531200	Weak transcription	Right Ventricle	heart
26	chr9:524600-531800	Weak transcription	Fetal Lung	lung
27	chr9:524800-525400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:524800-526200	Weak transcription	Pancreas	Pancrea
29	chr9:524800-527400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr9:524800-529600	Weak transcription	Fetal Heart	heart
31	chr9:524800-530600	Weak transcription	Brain Hippocampus Middle	brain
32	chr9:524800-530800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr9:524800-531200	Weak transcription	Aorta	Aorta
34	chr9:524800-531200	Weak transcription	Brain Anterior Caudate	brain
35	chr9:525400-526400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr9:525400-526400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr9:525400-526800	Strong transcription	Fetal Intestine Small	intestine
38	chr9:525400-532400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr9:526200-526400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:526200-526400	Enhancers	Pancreas	Pancrea
41	chr9:526400-527000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:526400-527000	Weak transcription	Pancreas	Pancrea
43	chr9:526400-528600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr9:526400-535000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:526800-528600	Weak transcription	Fetal Intestine Small	intestine
46	chr9:527000-527200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr9:527000-527400	Enhancers	Fetal Intestine Large	intestine
48	chr9:527000-527400	Enhancers	A549	lung
49	chr9:527000-527600	Enhancers	Pancreas	Pancrea
50	chr9:527000-527600	Enhancers	Psoas Muscle	Psoas

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