Variant report

Variant	nsv613019
Chromosome Location	chr9:526772-811618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3775)
CpG islands
(count:428)
Chromatin interactive
region (count:104)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3775 , 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	chr9:755679-756377	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:764021-764430	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
4	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
18	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
19	ARID3A	chr9:613790-614724	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	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr9:652937-653241	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	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
28	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
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	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
34	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
35	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
36	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
37	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
38	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
39	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
40	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
41	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
43	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
44	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
45	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
46	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
47	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
48	BHLHE40	chr9:694893-695215	A549	lung:	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:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:705143-705193	AG04449	skin:	fetal
2	chr9:705143-705193	AG04449	skin:	fetal
3	chr9:574312-574362	HRE	kidney:	n/a
4	chr9:574312-574362	SAEC	small airway:	n/a
5	chr9:707410-707460	HCM	heart:	n/a
6	chr9:705143-705193	AG09319	gingival:	n/a
7	chr9:707387-707437	NHBE	bronchial:	n/a
8	chr9:574312-574362	SK-N-SH_RA	brain:	n/a
9	chr9:574312-574362	BE2_C	brain:	n/a
10	chr9:705143-705193	AG04450	lung:	fetal
11	chr9:707410-707460	HEK293	kidney:	embryo
12	chr9:707410-707460	H1-hESC	embryonic stem cell:	embryo
13	chr9:714269-714319	HIPEpiC	eye:	n/a
14	chr9:707387-707437	HRCEpiC	kidney:	n/a
15	chr9:705143-705193	PANC-1	pancreas:	n/a
16	chr9:707166-707216	AG04450	lung:	fetal
17	chr9:707166-707216	AG10803	skin:	n/a
18	chr9:707166-707216	T-47D	breast:	n/a
19	chr9:714269-714319	CMK	blood:	n/a
20	chr9:707387-707437	H1-hESC	embryonic stem cell:	embryo
21	chr9:707410-707460	CMK	blood:	n/a
22	chr9:714269-714319	SAEC	small airway:	n/a
23	chr9:707166-707216	SK-N-SH	brain:	n/a
24	chr9:574312-574362	GM12892	blood:	n/a
25	chr9:714269-714319	NB4	blood:	n/a
26	chr9:574312-574362	Hepatocyte	liver:	n/a
27	chr9:707410-707460	ECC-1	luminal epithelium:	n/a
28	chr9:707387-707437	HIPEpiC	eye:	n/a
29	chr9:761482-761532	HAEpiC	amniotic membrane:	n/a
30	chr9:707387-707437	U87	brain:	n/a
31	chr9:574312-574362	RPTEC	kidney:	n/a
32	chr9:707387-707437	SAEC	small airway:	n/a
33	chr9:574312-574362	MCF10A-Er-Src	breast:	n/a
34	chr9:574312-574362	HUVEC	blood vessel:	n/a
35	chr9:574312-574362	BJ	skin:	n/a
36	chr9:714269-714319	HCPEpiC	choroid plexus:	n/a
37	chr9:761482-761532	NT2-D1	testis:	n/a
38	chr9:761482-761532	BE2_C	brain:	n/a
39	chr9:761482-761532	GM12878	blood:	n/a
40	chr9:714269-714319	HRCEpiC	kidney:	n/a
41	chr9:707387-707437	AG04450	lung:	fetal
42	chr9:574312-574362	HCPEpiC	choroid plexus:	n/a
43	chr9:761482-761532	HPAEpiC	pulmonary alveolar:	n/a
44	chr9:761482-761532	RPTEC	kidney:	n/a
45	chr9:714269-714319	AG04449	skin:	fetal
46	chr9:707166-707216	HepG2	liver:	n/a
47	chr9:761482-761532	CMK	blood:	n/a
48	chr9:707387-707437	AG10803	skin:	n/a
49	chr9:574312-574362	HCM	heart:	n/a
50	chr9:707166-707216	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
2	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
3	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
4	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
5	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
6	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
7	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
8	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
9	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
10	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
11	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
12	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
13	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
14	chr9:705245..708353-chr9:743847..747461,3	MCF-7	breast:
15	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
16	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
17	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
18	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
19	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
20	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
21	chr8:128752586..128753455-chr9:706903..707668,2	NB4	blood:
22	chr9:730043..732840-chr9:737557..739917,2	MCF-7	breast:
23	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
24	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
25	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
26	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
27	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
28	chr9:706377..708156-chr9:805249..808005,2	MCF-7	breast:
29	chr16:1239384..1239884-chr9:736833..737597,2	MCF-7	breast:
30	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
31	chr9:697287..699295-chr9:705065..707332,2	K562	blood:
32	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
33	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
34	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
35	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
36	chr17:17584235..17586582-chr9:741151..743803,2	MCF-7	breast:
37	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
38	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
39	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
40	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
41	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
42	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
43	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
44	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
45	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
46	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
47	chr9:706307..708254-chr9:737100..740465,4	MCF-7	breast:
48	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
49	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
50	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:

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

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

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

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

Extended variants
information (count: 16638 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:16638 , 50 per page) page: 1 2 3 4 5 6 7 ... 333

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9407292	chr9:526772-526773	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115219051	chr9:526787-526788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574020334	chr9:526839-526840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543023315	chr9:526856-526857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142181356	chr9:526872-526873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576452122	chr9:526882-526883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545446921	chr9:526904-526905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367838742	chr9:526906-526907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113030565	chr9:526907-526908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34451693	chr9:526918-526919	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs9408610	chr9:526919-526920	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs373588963	chr9:526932-526933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145774492	chr9:526944-526945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184597363	chr9:526950-526951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75752263	chr9:526970-526971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148172907	chr9:527024-527025	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189242914	chr9:527040-527041	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141984535	chr9:527096-527097	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75646607	chr9:527101-527102	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571269818	chr9:527138-527139	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533958379	chr9:527157-527158	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10974992	chr9:527180-527181	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs12682818	chr9:527220-527221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182122792	chr9:527226-527227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375572005	chr9:527252-527253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576342818	chr9:527288-527289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142932692	chr9:527293-527294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376160444	chr9:527294-527295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35256853	chr9:527313-527314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs56258904	chr9:527316-527317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113604712	chr9:527317-527318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185138267	chr9:527356-527357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558978541	chr9:527362-527363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572483133	chr9:527364-527365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190039376	chr9:527370-527371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561194460	chr9:527378-527379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368411422	chr9:527387-527388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181113109	chr9:527388-527389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543668591	chr9:527393-527394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386731406	chr9:527407-527408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142642634	chr9:527409-527410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571523034	chr9:527410-527411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531302764	chr9:527417-527418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375264686	chr9:527420-527421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368341294	chr9:527421-527422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150618175	chr9:527434-527435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139669049	chr9:527442-527443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527428156	chr9:527451-527452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535616577	chr9:527457-527458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185360868	chr9:527487-527488	Weak transcription Enhancers	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:7635 , 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	chr9:524800-527400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr9:524800-529600	Weak transcription	Fetal Heart	heart
25	chr9:524800-530600	Weak transcription	Brain Hippocampus Middle	brain
26	chr9:524800-530800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr9:524800-531200	Weak transcription	Aorta	Aorta
28	chr9:524800-531200	Weak transcription	Brain Anterior Caudate	brain
29	chr9:525400-526800	Strong transcription	Fetal Intestine Small	intestine
30	chr9:525400-532400	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr9:526400-527000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr9:526400-527000	Weak transcription	Pancreas	Pancrea
33	chr9:526400-528600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:526400-535000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr9:526800-528600	Weak transcription	Fetal Intestine Small	intestine
36	chr9:527000-527200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr9:527000-527400	Enhancers	Fetal Intestine Large	intestine
38	chr9:527000-527400	Enhancers	A549	lung
39	chr9:527000-527600	Enhancers	Pancreas	Pancrea
40	chr9:527000-527600	Enhancers	Psoas Muscle	Psoas
41	chr9:527200-529600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:527400-527600	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr9:527400-529600	Weak transcription	A549	lung
44	chr9:527400-532400	Weak transcription	Fetal Intestine Large	intestine
45	chr9:527600-530800	Weak transcription	Pancreas	Pancrea
46	chr9:527600-534800	Weak transcription	Psoas Muscle	Psoas
47	chr9:527600-535000	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr9:528000-537400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr9:528600-529000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr9:528600-529400	Strong transcription	Fetal Intestine Small	intestine

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