Variant report

Variant	nsv1016139
Chromosome Location	chr9:731139-827580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:792615-792973	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:764021-764430	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:755679-756377	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
7	BACH1	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
8	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
9	BATF	chr9:755709-756109	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
10	BATF	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
11	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
16	BRCA1	chr9:756272-756352	HepG2	liver:	n/a	n/a
17	BRCA1	chr9:763966-764464	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr9:763894-764606	HCT-116	colon:	n/a	n/a
19	CEBPB	chr9:792603-793029	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
20	CEBPB	chr9:819788-820128	IMR90	lung:	n/a	chr9:819810-819821
21	CEBPB	chr9:734751-735614	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:745733-746086	HepG2	liver:	n/a	chr9:745902-745913
23	CEBPB	chr9:744778-744956	HepG2	liver:	n/a	chr9:744883-744894
24	CEBPB	chr9:798763-798775	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:792604-793040	MCF-7	breast:	n/a	chr9:792818-792829 chr9:792819-792830
26	CEBPB	chr9:745827-745954	HepG2	liver:	n/a	chr9:745902-745913
27	CEBPB	chr9:755729-756376	HepG2	liver:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
28	CEBPB	chr9:758200-758514	HepG2	liver:	n/a	chr9:758338-758349
29	CEBPB	chr9:737783-737987	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:792649-793016	IMR90	lung:	n/a	chr9:792818-792829 chr9:792819-792830
31	CEBPB	chr9:755719-756399	IMR90	lung:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
32	CEBPB	chr9:758200-758516	IMR90	lung:	n/a	chr9:758338-758349
33	CEBPB	chr9:737754-737954	A549	lung:	n/a	n/a
34	CEBPB	chr9:755785-756371	A549	lung:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
35	CEBPB	chr9:755733-756385	HepG2	liver:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
36	CEBPB	chr9:792635-792995	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
37	CEBPB	chr9:812281-812423	HepG2	liver:	n/a	chr9:812339-812350
38	CEBPB	chr9:792676-792923	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
39	CEBPB	chr9:758990-759190	IMR90	lung:	n/a	chr9:759082-759093
40	CEBPB	chr9:758217-758477	Hela-S3	cervix:	n/a	chr9:758338-758349
41	CEBPB	chr9:755941-756445	MCF-7	breast:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
42	CEBPB	chr9:792618-793073	HepG2	liver:	n/a	chr9:792818-792829 chr9:792819-792830
43	CEBPB	chr9:755745-756382	Hela-S3	cervix:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
44	CEBPB	chr9:737825-737895	K562	blood:	n/a	n/a
45	CEBPB	chr9:792687-793022	Hela-S3	cervix:	n/a	chr9:792818-792829 chr9:792819-792830
46	CEBPB	chr9:737718-738042	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:761422-761787	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:759008-759187	HepG2	liver:	n/a	chr9:759082-759093
49	CEBPB	chr9:756016-756351	H1-hESC	embryonic stem cell:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
50	CEBPB	chr9:755861-756461	A549	lung:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:826657-826707	NB4	blood:	n/a
2	chr9:826657-826707	NB4	blood:	n/a
3	chr9:761482-761532	NHDF-neo	bronchial:	n/a
4	chr9:761482-761532	GM12878	blood:	n/a
5	chr9:826657-826707	HL-60	blood:	n/a
6	chr9:761482-761532	HRPEpiC	eye:	n/a
7	chr9:826657-826707	NHDF-neo	bronchial:	n/a
8	chr9:826657-826707	HMEC	breast:	n/a
9	chr9:826657-826707	NHBE	bronchial:	n/a
10	chr9:826657-826707	GM12878	blood:	n/a
11	chr9:826657-826707	Jurkat	blood:	n/a
12	chr9:761482-761532	H1-hESC	embryonic stem cell:	embryo
13	chr9:761482-761532	ECC-1	luminal epithelium:	n/a
14	chr9:761482-761532	ovcar-3	ovarian:	n/a
15	chr9:761482-761532	GM12892	blood:	n/a
16	chr9:826657-826707	CMK	blood:	n/a
17	chr9:761482-761532	MCF10A-Er-Src	breast:	n/a
18	chr9:761482-761532	HMEC	breast:	n/a
19	chr9:761482-761532	Hela-S3	cervix:	n/a
20	chr9:761482-761532	RPTEC	kidney:	n/a
21	chr9:826657-826707	LNCaP	prostate:	n/a
22	chr9:826657-826707	GM12892	blood:	n/a
23	chr9:761482-761532	HNPCEpiC	eye:	n/a
24	chr9:826657-826707	HRE	kidney:	n/a
25	chr9:826657-826707	ovcar-3	ovarian:	n/a
26	chr9:826657-826707	SKMC	muscle:	n/a
27	chr9:826657-826707	NH-A	brain:	n/a
28	chr9:826657-826707	HPAEpiC	pulmonary alveolar:	n/a
29	chr9:826657-826707	HRPEpiC	eye:	n/a
30	chr9:761482-761532	Caco-2	colon:	n/a
31	chr9:761482-761532	NHBE	bronchial:	n/a
32	chr9:826657-826707	HepG2	liver:	n/a
33	chr9:761482-761532	AoSMC	blood vessel:	n/a
34	chr9:826657-826707	AG10803	skin:	n/a
35	chr9:761482-761532	BJ	skin:	n/a
36	chr9:826657-826707	SAEC	small airway:	n/a
37	chr9:826657-826707	RPTEC	kidney:	n/a
38	chr9:826657-826707	HNPCEpiC	eye:	n/a
39	chr9:826657-826707	GM06990	blood:	n/a
40	chr9:761482-761532	NB4	blood:	n/a
41	chr9:826657-826707	Hepatocyte	liver:	n/a
42	chr9:761482-761532	AG09309	skin:	n/a
43	chr9:826657-826707	HEK293	kidney:	embryo
44	chr9:826657-826707	Caco-2	colon:	n/a
45	chr9:761482-761532	AG10803	skin:	n/a
46	chr9:826657-826707	PANC-1	pancreas:	n/a
47	chr9:826657-826707	HCPEpiC	choroid plexus:	n/a
48	chr9:761482-761532	SK-N-MC	brain:	n/a
49	chr9:761482-761532	HRE	kidney:	n/a
50	chr9:761482-761532	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
2	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
3	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
4	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
5	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
6	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
7	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
8	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
9	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
10	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
11	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
12	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
13	chr9:763806..764607-chr9:806256..807153,5	MCF-7	breast:
14	chr9:385566..386417-chr9:764222..764740,2	MCF-7	breast:
15	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
16	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
17	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
18	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
19	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
20	chr9:730043..732840-chr9:737557..739917,2	MCF-7	breast:
21	chr9:705245..708353-chr9:743847..747461,3	MCF-7	breast:
22	chr9:706307..708254-chr9:737100..740465,4	MCF-7	breast:
23	chr9:782884..784766-chr9:785783..787661,2	MCF-7	breast:
24	chr9:706377..708156-chr9:805249..808005,2	MCF-7	breast:
25	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
26	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
27	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
28	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
29	chr17:17584235..17586582-chr9:741151..743803,2	MCF-7	breast:
30	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
31	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
32	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
33	chr16:1239384..1239884-chr9:736833..737597,2	MCF-7	breast:
34	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
35	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
36	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
37	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
38	chr9:763791..764994-chr9:806035..807196,9	MCF-7	breast:
39	chr9:763938..764768-chr9:1004823..1005723,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-5	chr9:755232-755507	XLOC_007629
2	lnc-C9orf66-4	chr9:761299-761551	XLOC_007628
3	lnc-C9orf66-4	chr9:749336-749496	XLOC_007628
4	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
5	lnc-C9orf66-5	chr9:752722-752856	XLOC_007629
6	lnc-KANK1-1	chr9:747412-747469	NONHSAT129937
7	lnc-KANK1-1	chr9:746431-746497	NONHSAT129937
8	lnc-KANK1-1	chr9:748000-751056	NONHSAT129937
9	lnc-C9orf66-4	chr9:749336-749509	XLOC_007628
10	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
11	lnc-KANK1-1	chr9:747272-747365	NONHSAT129937

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

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

Extended variants
information (count: 4723 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:4723 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528965130	chr9:731151-731152	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs376408309	chr9:731157-731158	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs114209322	chr9:731164-731165	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112517899	chr9:731173-731174	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369696901	chr9:731204-731205	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs562561638	chr9:731208-731209	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs74458120	chr9:731212-731213	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551710375	chr9:731216-731217	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs571520878	chr9:731217-731218	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs138899296	chr9:731229-731230	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs141422149	chr9:731265-731266	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs184585076	chr9:731275-731276	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547802424	chr9:731277-731278	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs114657844	chr9:731288-731289	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs377246939	chr9:731315-731316	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10491591	chr9:731332-731333	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs139883316	chr9:731349-731350	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs143876266	chr9:731350-731351	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs539174094	chr9:731358-731359	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558868154	chr9:731366-731367	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs188905792	chr9:731367-731368	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539874289	chr9:731387-731388	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs569493149	chr9:731390-731391	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs77963287	chr9:731400-731401	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs75742299	chr9:731420-731421	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs562564050	chr9:731445-731446	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs147245056	chr9:731451-731452	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs551599434	chr9:731483-731484	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs565218324	chr9:731485-731486	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs527571229	chr9:731486-731487	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs547842209	chr9:731487-731488	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567577772	chr9:731522-731523	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs530072213	chr9:731531-731532	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs140847052	chr9:731532-731533	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs78267743	chr9:731535-731536	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs538884193	chr9:731558-731559	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs142330587	chr9:731569-731570	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566059757	chr9:731572-731573	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535006308	chr9:731581-731582	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs181288410	chr9:731600-731601	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573563849	chr9:731605-731606	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542564029	chr9:731627-731628	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556033365	chr9:731632-731633	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs185689283	chr9:731639-731640	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374191277	chr9:731683-731684	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs150566969	chr9:731689-731690	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs376271406	chr9:731705-731706	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565054222	chr9:731707-731708	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs572512028	chr9:731842-731843	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs527456859	chr9:731852-731853	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:712000-731600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr9:712000-734800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr9:712200-741200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr9:712800-740400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr9:713000-740400	Weak transcription	Spleen	Spleen
6	chr9:713000-740600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr9:713000-743400	Weak transcription	Thymus	Thymus
8	chr9:713400-731200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr9:713400-731200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr9:713400-735800	Weak transcription	Colonic Mucosa	Colon
11	chr9:713600-734800	Weak transcription	A549	lung
12	chr9:714000-731200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:717400-734200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr9:720600-733800	Weak transcription	Lung	lung
15	chr9:720600-739000	Weak transcription	Small Intestine	intestine
16	chr9:720800-731200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr9:720800-731200	Weak transcription	Esophagus	oesophagus
18	chr9:720800-734200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr9:720800-744000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:722800-733400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:723200-731200	Weak transcription	Psoas Muscle	Psoas
22	chr9:723200-731600	Weak transcription	Colon Smooth Muscle	Colon
23	chr9:724400-731200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr9:726600-731200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:726600-742800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:726800-733600	Weak transcription	Right Atrium	heart
27	chr9:727400-734800	Weak transcription	Fetal Brain Female	brain
28	chr9:727400-737400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr9:727600-731400	Strong transcription	HepG2	liver
30	chr9:727600-733000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:727600-742000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:728000-731200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr9:728000-734600	Weak transcription	Fetal Heart	heart
34	chr9:728200-733800	Strong transcription	Adipose Nuclei	Adipose
35	chr9:728200-734800	Strong transcription	HMEC	breast
36	chr9:728400-733600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr9:728400-733800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:728400-737400	Strong transcription	Liver	Liver
39	chr9:728600-731200	Weak transcription	Pancreas	Pancrea
40	chr9:728800-733800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr9:728800-738600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:728800-745000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:728800-745000	Weak transcription	Stomach Mucosa	stomach
44	chr9:729000-732800	Strong transcription	NHDF-Ad	bronchial
45	chr9:729000-734000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:729000-734800	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr9:729200-734200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr9:729200-734600	Weak transcription	Fetal Lung	lung
49	chr9:729200-737800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:729200-737800	Strong transcription	NHEK	skin

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