Variant report

Variant	nsv615747
Chromosome Location	chr9:136852501-136877628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1592)
CpG islands
(count:979)
Chromatin interactive
region (count:71)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136859562-136859782	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:136876031-136876182	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:136856048-136856079	HepG2	liver:	n/a	n/a
4	BACH1	chr9:136858165-136858241	K562	blood:	n/a	n/a
5	BACH1	chr9:136857281-136858367	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:136856855-136856872	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:136856324-136856351	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr9:136857104-136857688	GM12878	blood:	n/a	chr9:136857527-136857540 chr9:136857667-136857680 chr9:136857587-136857600
9	BCL3	chr9:136857966-136858629	A549	lung:	n/a	chr9:136858041-136858050 chr9:136858023-136858032 chr9:136858029-136858038
10	BCLAF1	chr9:136857182-136857925	GM12878	blood:	n/a	chr9:136857527-136857540 chr9:136857722-136857735 chr9:136857667-136857680 chr9:136857587-136857600 chr9:136857703-136857716
11	BCLAF1	chr9:136857949-136858391	GM12878	blood:	n/a	chr9:136858041-136858050 chr9:136858023-136858032 chr9:136858029-136858038
12	BHLHE40	chr9:136857175-136857795	GM12878	blood:	n/a	chr9:136857723-136857739
13	BHLHE40	chr9:136869547-136869987	K562	blood:	n/a	chr9:136869715-136869728 chr9:136869957-136869973 chr9:136869906-136869915 chr9:136869716-136869725
14	BHLHE40	chr9:136857536-136857643	K562	blood:	n/a	n/a
15	BHLHE40	chr9:136869497-136870038	HepG2	liver:	n/a	chr9:136869715-136869728 chr9:136869957-136869973 chr9:136869906-136869915 chr9:136869716-136869725
16	BHLHE40	chr9:136859506-136859800	K562	blood:	n/a	n/a
17	BHLHE40	chr9:136858022-136858718	GM12878	blood:	n/a	chr9:136858292-136858308
18	BHLHE40	chr9:136859537-136859868	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:136857238-136857657	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:136858375-136858412	K562	blood:	n/a	n/a
21	BHLHE40	chr9:136856410-136856656	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:136869721-136869754	GM12878	blood:	n/a	n/a
23	BRCA1	chr9:136856472-136856482	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr9:136858624-136858795	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr9:136857229-136857386	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr9:136859571-136859661	HepG2	liver:	n/a	n/a
27	BRCA1	chr9:136859495-136859859	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr9:136859697-136859701	GM12878	blood:	n/a	n/a
29	CCNT2	chr9:136857387-136858522	K562	blood:	n/a	chr9:136858030-136858039 chr9:136858444-136858453
30	CEBPB	chr9:136859569-136859830	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:136862116-136862444	IMR90	lung:	n/a	chr9:136862275-136862286
32	CEBPB	chr9:136857190-136857515	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:136858693-136858716	K562	blood:	n/a	n/a
34	CEBPB	chr9:136856052-136856100	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:136862155-136862420	Hela-S3	cervix:	n/a	chr9:136862275-136862286
36	CEBPB	chr9:136859558-136859784	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:136856519-136856548	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:136864401-136864645	IMR90	lung:	n/a	chr9:136864525-136864536
39	CEBPB	chr9:136858175-136858310	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr9:136862197-136862411	HepG2	liver:	n/a	chr9:136862275-136862286
41	CEBPB	chr9:136858000-136858845	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr9:136856033-136856632	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:136858552-136858776	HepG2	liver:	n/a	n/a
44	CEBPD	chr9:136858491-136858779	HepG2	liver:	n/a	n/a
45	CEBPD	chr9:136857224-136858245	HepG2	liver:	n/a	n/a
46	CHD1	chr9:136859440-136860013	IMR90	lung:	n/a	n/a
47	CHD1	chr9:136857138-136857719	GM12878	blood:	n/a	n/a
48	CHD1	chr9:136856264-136856393	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr9:136859517-136859839	GM12878	blood:	n/a	n/a
50	CHD1	chr9:136858037-136858270	GM12878	blood:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136858308-136858358	HepG2	liver:	n/a
2	chr9:136876905-136876955	HRPEpiC	eye:	n/a
3	chr9:136877010-136877060	Caco-2	colon:	n/a
4	chr9:136858308-136858358	HepG2	liver:	n/a
5	chr9:136876905-136876955	HRPEpiC	eye:	n/a
6	chr9:136877010-136877060	Caco-2	colon:	n/a
7	chr9:136873539-136873589	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:136877010-136877060	ECC-1	luminal epithelium:	n/a
9	chr9:136877010-136877060	Hela-S3	cervix:	n/a
10	chr9:136857190-136857240	A549	lung:	n/a
11	chr9:136873539-136873589	U87	brain:	n/a
12	chr9:136876905-136876955	GM12891	blood:	n/a
13	chr9:136869371-136869421	HCT-116	colon:	n/a
14	chr9:136860187-136860237	HRE	kidney:	n/a
15	chr9:136857244-136857294	HCT-116	colon:	n/a
16	chr9:136856435-136856485	MCF10A-Er-Src	breast:	n/a
17	chr9:136857190-136857240	NHDF-neo	bronchial:	n/a
18	chr9:136876905-136876955	HepG2	liver:	n/a
19	chr9:136858680-136858730	NT2-D1	testis:	n/a
20	chr9:136857244-136857294	SKMC	muscle:	n/a
21	chr9:136876366-136876416	SK-N-SH_RA	brain:	n/a
22	chr9:136869371-136869421	SK-N-SH	brain:	n/a
23	chr9:136858163-136858213	ProgFib	skin:	n/a
24	chr9:136873539-136873589	BJ	skin:	n/a
25	chr9:136856352-136856402	HCM	heart:	n/a
26	chr9:136860187-136860237	RPTEC	kidney:	n/a
27	chr9:136876366-136876416	NB4	blood:	n/a
28	chr9:136858673-136858723	SK-N-SH_RA	brain:	n/a
29	chr9:136858680-136858730	ECC-1	luminal epithelium:	n/a
30	chr9:136876366-136876416	NHBE	bronchial:	n/a
31	chr9:136858673-136858723	HRE	kidney:	n/a
32	chr9:136857244-136857294	HNPCEpiC	eye:	n/a
33	chr9:136858308-136858358	AG04450	lung:	fetal
34	chr9:136858163-136858213	HUVEC	blood vessel:	n/a
35	chr9:136855902-136855952	Caco-2	colon:	n/a
36	chr9:136873539-136873589	HRCEpiC	kidney:	n/a
37	chr9:136873539-136873589	Jurkat	blood:	n/a
38	chr9:136876905-136876955	HNPCEpiC	eye:	n/a
39	chr9:136860187-136860237	U87	brain:	n/a
40	chr9:136857244-136857294	PANC-1	pancreas:	n/a
41	chr9:136876905-136876955	ovcar-3	ovarian:	n/a
42	chr9:136856435-136856485	ovcar-3	ovarian:	n/a
43	chr9:136858673-136858723	HRCEpiC	kidney:	n/a
44	chr9:136861819-136861869	Jurkat	blood:	n/a
45	chr9:136869371-136869421	Jurkat	blood:	n/a
46	chr9:136860187-136860237	HEEpiC	esophagus:	n/a
47	chr9:136869371-136869421	GM12891	blood:	n/a
48	chr9:136877010-136877060	MCF10A-Er-Src	breast:	n/a
49	chr9:136869371-136869421	ECC-1	luminal epithelium:	n/a
50	chr9:136873539-136873589	HEK293	kidney:	embryo

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:136857648..136860079-chr9:136868960..136870875,2	MCF-7	breast:
2	chr9:136835959..136838306-chr9:136857880..136859486,2	MCF-7	breast:
3	chr9:136856335..136860882-chr9:136888369..136892368,8	MCF-7	breast:
4	chr9:136657265..136659232-chr9:136854243..136855846,2	K562	blood:
5	chr9:136790195..136791923-chr9:136853934..136856006,2	MCF-7	breast:
6	chr9:136866726..136869330-chr9:136873056..136875890,3	MCF-7	breast:
7	chr17:58677435..58680394-chr9:136857896..136860386,2	MCF-7	breast:
8	chr9:136747429..136748291-chr9:136859497..136860075,2	MCF-7	breast:
9	chr9:136706030..136708990-chr9:136860281..136862454,2	MCF-7	breast:
10	chr9:136647409..136647939-chr9:136859642..136860182,3	K562	blood:
11	chr9:136862110..136863707-chr9:136863725..136867446,4	MCF-7	breast:
12	chr9:136594711..136597550-chr9:136858767..136860355,2	MCF-7	breast:
13	chr9:136857193..136859735-chr9:136888278..136891342,4	MCF-7	breast:
14	chr9:136655962..136656512-chr9:136858875..136859685,2	K562	blood:
15	chr9:136751034..136753056-chr9:136851311..136853643,2	MCF-7	breast:
16	chr9:136655644..136657543-chr9:136859054..136861724,2	K562	blood:
17	chr9:136819042..136820561-chr9:136859120..136860817,2	MCF-7	breast:
18	chr9:136868478..136870718-chr9:136870776..136873148,2	K562	blood:
19	chr9:136662303..136663068-chr9:136859673..136860648,2	MCF-7	breast:
20	chr9:136646919..136648935-chr9:136858713..136860466,10	MCF-7	breast:
21	chr9:136867977..136869664-chr9:136870201..136872512,2	MCF-7	breast:
22	chr9:136839997..136844319-chr9:136851053..136854251,5	MCF-7	breast:
23	chr1:16678857..16679483-chr9:136857773..136858655,2	Hela-S3	cervix:
24	chr9:136849949..136852879-chr9:136857069..136859221,2	K562	blood:
25	chr9:136859325..136860777-chr9:136964002..136965283,7	MCF-7	breast:
26	chr9:136592345..136593069-chr9:136859637..136860159,2	MCF-7	breast:
27	chr9:136856397..136858189-chr9:136860981..136863697,2	K562	blood:
28	chr9:136867977..136869664-chr9:136870201..136872512,2	MCF-7	breast:
29	chr9:136647007..136648956-chr9:136858795..136860235,12	MCF-7	breast:
30	chr9:136855194..136860597-chr9:136929703..136933650,7	MCF-7	breast:
31	chr22:43010797..43011769-chr9:136856743..136857657,2	Hela-S3	cervix:
32	chr9:136372726..136374611-chr9:136854336..136856756,2	MCF-7	breast:
33	chr9:136657461..136661655-chr9:136857893..136859866,4	K562	blood:
34	chr9:136821904..136824368-chr9:136852633..136855112,2	MCF-7	breast:
35	chr9:136856689..136859629-chr9:136860948..136863697,2	K562	blood:
36	chr9:136647156..136647722-chr9:136857760..136858312,2	MCF-7	breast:
37	chr17:56084236..56085114-chr9:136858119..136858641,2	Hela-S3	cervix:
38	chr9:136608029..136608531-chr9:136858192..136859169,2	MCF-7	breast:
39	chr9:136679694..136681677-chr9:136851207..136853977,2	MCF-7	breast:
40	chr20:48329316..48329843-chr9:136855861..136856467,2	Hela-S3	cervix:
41	chr9:136866726..136869330-chr9:136873056..136875890,3	MCF-7	breast:
42	chr17:41465782..41466571-chr9:136857818..136858531,2	Hela-S3	cervix:
43	chr9:136607827..136608773-chr9:136859602..136860351,4	MCF-7	breast:
44	chr9:136591900..136594207-chr9:136858637..136860236,2	MCF-7	breast:
45	chr9:136815020..136816601-chr9:136860068..136862429,2	MCF-7	breast:
46	chr9:136859431..136860674-chr9:136964030..136964900,5	MCF-7	breast:
47	chr9:136855434..136861951-chr9:136862866..136866695,10	MCF-7	breast:
48	chr17:7387387..7388059-chr9:136856964..136857786,2	Hela-S3	cervix:
49	chr9:136741297..136743504-chr9:136863564..136865596,2	MCF-7	breast:
50	chr9:136657412..136658751-chr9:136858523..136860164,12	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR5-7	chr9:136857728-136861324	NONHSAT135347

No data

Variant related genes	Relation type
VAV2	TF binding region
VAV2	CpG island
ENSG00000170836	chromatin interactions
ENSG00000169925	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000037637	chromatin interactions
ENSG00000055070	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000160293	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000123453	chromatin interactions
ENSG00000235106	chromatin interactions

Extended variants
information (count: 1108 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1108 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2519824	chr9:136852501-136852502	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573936056	chr9:136852544-136852545	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185613414	chr9:136852546-136852547	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141131194	chr9:136852574-136852575	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543134749	chr9:136852588-136852589	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72764881	chr9:136852615-136852616	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs150746884	chr9:136852616-136852617	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs369484859	chr9:136852620-136852621	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577979308	chr9:136852623-136852624	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545070809	chr9:136852624-136852625	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563457163	chr9:136852646-136852647	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530968590	chr9:136852652-136852653	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556403332	chr9:136852653-136852654	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2519825	chr9:136852667-136852668	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs528773302	chr9:136852721-136852722	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547012698	chr9:136852728-136852729	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs137957367	chr9:136852729-136852730	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538663231	chr9:136852771-136852772	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539237352	chr9:136852772-136852773	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143003519	chr9:136852775-136852776	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs3780799	chr9:136852803-136852804	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs2789863	chr9:136852820-136852821	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs113843108	chr9:136852839-136852840	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377124387	chr9:136852875-136852876	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534387315	chr9:136852881-136852882	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2789864	chr9:136852891-136852892	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs34288869	chr9:136852932-136852933	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577581216	chr9:136852954-136852955	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545010375	chr9:136853044-136853045	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563393933	chr9:136853062-136853063	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191435005	chr9:136853102-136853103	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539701845	chr9:136853114-136853115	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542795994	chr9:136853164-136853165	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561517334	chr9:136853246-136853247	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183631740	chr9:136853254-136853255	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556434497	chr9:136853282-136853283	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547245908	chr9:136853306-136853307	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565458570	chr9:136853339-136853340	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374128122	chr9:136853350-136853351	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146120986	chr9:136853357-136853358	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550600786	chr9:136853369-136853370	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2789865	chr9:136853379-136853380	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs529797051	chr9:136853390-136853391	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536076663	chr9:136853397-136853398	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13286988	chr9:136853442-136853443	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs548004710	chr9:136853445-136853446	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566629824	chr9:136853448-136853449	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs533762960	chr9:136853588-136853589	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs140200484	chr9:136853642-136853643	Enhancers Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs72764882	chr9:136853660-136853661	Enhancers Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136835800-136854800	Weak transcription	A549	lung
2	chr9:136837400-136854800	Weak transcription	HMEC	breast
3	chr9:136838000-136854800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:136840000-136854800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr9:136840400-136854800	Weak transcription	Hela-S3	cervix
6	chr9:136840800-136852600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:136844200-136855800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr9:136844200-136856000	Weak transcription	Small Intestine	intestine
9	chr9:136845200-136855000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:136845400-136855000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:136845600-136854800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr9:136845600-136855000	Weak transcription	NHDF-Ad	bronchial
13	chr9:136845800-136854800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:136845800-136855000	Weak transcription	Esophagus	oesophagus
15	chr9:136845800-136855000	Weak transcription	NHLF	lung
16	chr9:136845800-136855400	Weak transcription	Right Atrium	heart
17	chr9:136845800-136855400	Weak transcription	Osteobl	bone
18	chr9:136845800-136855600	Weak transcription	HSMMtube	muscle
19	chr9:136846000-136855800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr9:136846200-136854800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr9:136846200-136855600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr9:136846400-136855000	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr9:136846400-136856000	Weak transcription	Fetal Kidney	kidney
24	chr9:136846800-136855400	Weak transcription	Right Ventricle	heart
25	chr9:136847000-136855000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:136847000-136855200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr9:136847000-136855200	Weak transcription	HSMM	muscle
28	chr9:136847400-136852800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr9:136847400-136854800	Weak transcription	Lung	lung
30	chr9:136847400-136855000	Weak transcription	Spleen	Spleen
31	chr9:136847600-136854800	Weak transcription	Liver	Liver
32	chr9:136847600-136855400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr9:136847800-136853200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:136847800-136855000	Weak transcription	Colonic Mucosa	Colon
35	chr9:136847800-136855400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:136848400-136853200	Weak transcription	Fetal Lung	lung
37	chr9:136848400-136855400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:136848600-136855000	Weak transcription	Fetal Muscle Leg	muscle
39	chr9:136848800-136852600	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr9:136848800-136853400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:136848800-136854800	Weak transcription	Fetal Brain Female	brain
42	chr9:136848800-136855000	Weak transcription	Fetal Stomach	stomach
43	chr9:136849600-136852600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr9:136850200-136854800	Genic enhancers	HepG2	liver
45	chr9:136850400-136852600	Weak transcription	Fetal Intestine Large	intestine
46	chr9:136850400-136852600	Strong transcription	Fetal Intestine Small	intestine
47	chr9:136850400-136854800	Weak transcription	Gastric	stomach
48	chr9:136850600-136854200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr9:136851000-136854800	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr9:136851200-136855000	Enhancers	Primary B cells from peripheral blood	blood

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