Variant report

Variant	nsv529475
Chromosome Location	chr9:10648009-11435662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1411)
CpG islands
(count:61)
Chromatin interactive
region (count:53)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1411 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:11064894-11065285	K562	blood:	n/a	n/a
2	ARID3A	chr9:11064055-11064488	K562	blood:	n/a	n/a
3	ATF1	chr9:11064943-11065293	K562	blood:	n/a	n/a
4	ATF2	chr9:10921560-10922106	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:10921652-10922120	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:11016111-11016284	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:10910431-10910585	K562	blood:	n/a	n/a
8	BACH1	chr9:11067007-11067064	K562	blood:	n/a	n/a
9	BACH1	chr9:10731396-10731463	K562	blood:	n/a	n/a
10	BCL11A	chr9:11038049-11038208	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr9:10921715-10922010	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr9:11338205-11338405	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:11065067-11065094	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:11064998-11065193	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:11064885-11065303	K562	blood:	n/a	n/a
16	BRCA1	chr9:11064953-11065285	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr9:11272473-11272479	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr9:11319527-11319802	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr9:11064529-11064729	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr9:11269115-11269340	K562	blood:	n/a	n/a
21	CBX3	chr9:11064870-11065315	K562	blood:	n/a	n/a
22	CEBPB	chr9:10929200-10929413	HepG2	liver:	n/a	chr9:10929234-10929247 chr9:10929234-10929245 chr9:10929234-10929247 chr9:10929293-10929304
23	CEBPB	chr9:11349171-11349446	HepG2	liver:	n/a	chr9:11349299-11349310
24	CEBPB	chr9:11084639-11084926	A549	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
25	CEBPB	chr9:11073751-11074022	IMR90	lung:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
26	CEBPB	chr9:11258134-11258408	HepG2	liver:	n/a	chr9:11258233-11258244
27	CEBPB	chr9:11217160-11217484	A549	lung:	n/a	n/a
28	CEBPB	chr9:11258112-11258312	K562	blood:	n/a	chr9:11258233-11258244
29	CEBPB	chr9:10959931-10960102	HepG2	liver:	n/a	chr9:10959996-10960007
30	CEBPB	chr9:10920298-10920309	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:11267017-11267301	K562	blood:	n/a	chr9:11267135-11267146
32	CEBPB	chr9:11407895-11408156	IMR90	lung:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
33	CEBPB	chr9:11022159-11022375	HepG2	liver:	n/a	chr9:11022289-11022300
34	CEBPB	chr9:11217166-11217491	IMR90	lung:	n/a	n/a
35	CEBPB	chr9:10906229-10906429	HepG2	liver:	n/a	chr9:10906301-10906312
36	CEBPB	chr9:10843733-10844029	HepG2	liver:	n/a	chr9:10843883-10843894
37	CEBPB	chr9:11357865-11358142	HepG2	liver:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
38	CEBPB	chr9:11084602-11084944	IMR90	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
39	CEBPB	chr9:11258136-11258368	H1-hESC	embryonic stem cell:	n/a	chr9:11258233-11258244
40	CEBPB	chr9:10921657-10922056	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr9:11258112-11258370	A549	lung:	n/a	chr9:11258233-11258244
42	CEBPB	chr9:11221528-11221540	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:11022120-11022420	Hela-S3	cervix:	n/a	chr9:11022289-11022300
44	CEBPB	chr9:11221350-11221590	IMR90	lung:	n/a	n/a
45	CEBPB	chr9:11073722-11074080	A549	lung:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
46	CEBPB	chr9:11294410-11294610	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:10870900-10871067	K562	blood:	n/a	chr9:10870983-10870994
48	CEBPB	chr9:10928603-10928846	HepG2	liver:	n/a	chr9:10928719-10928730
49	CEBPB	chr9:10800986-10801148	HepG2	liver:	n/a	chr9:10801096-10801107
50	CEBPB	chr9:11022160-11022402	A549	lung:	n/a	chr9:11022289-11022300

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:10966083-10966133	SAEC	small airway:	n/a
2	chr9:10966083-10966133	AG04449	skin:	fetal
3	chr9:10966083-10966133	H1-hESC	embryonic stem cell:	embryo
4	chr9:10966083-10966133	Hela-S3	cervix:	n/a
5	chr9:10966083-10966133	HRCEpiC	kidney:	n/a
6	chr9:10966083-10966133	HAEpiC	amniotic membrane:	n/a
7	chr9:10966083-10966133	NHBE	bronchial:	n/a
8	chr9:10966083-10966133	GM06990	blood:	n/a
9	chr9:10966083-10966133	NH-A	brain:	n/a
10	chr9:10966083-10966133	GM12891	blood:	n/a
11	chr9:10966083-10966133	SK-N-MC	brain:	n/a
12	chr9:10966083-10966133	NHDF-neo	bronchial:	n/a
13	chr9:10966083-10966133	NT2-D1	testis:	n/a
14	chr9:10966083-10966133	HEK293	kidney:	embryo
15	chr9:10966083-10966133	GM19239	blood:	n/a
16	chr9:10966083-10966133	ProgFib	skin:	n/a
17	chr9:10966083-10966133	PrEC	prostate:	n/a
18	chr9:10966083-10966133	IMR90	lung:	fetal
19	chr9:10966083-10966133	GM12878	blood:	n/a
20	chr9:10966083-10966133	HCF	heart:	n/a
21	chr9:10966083-10966133	HCPEpiC	choroid plexus:	n/a
22	chr9:10966083-10966133	ECC-1	luminal epithelium:	n/a
23	chr9:10966083-10966133	AoSMC	blood vessel:	n/a
24	chr9:10966083-10966133	Jurkat	blood:	n/a
25	chr9:10966083-10966133	HEEpiC	esophagus:	n/a
26	chr9:10966083-10966133	MCF10A-Er-Src	breast:	n/a
27	chr9:10966083-10966133	SK-N-SH	brain:	n/a
28	chr9:10966083-10966133	AG10803	skin:	n/a
29	chr9:10966083-10966133	HCM	heart:	n/a
30	chr9:10966083-10966133	PANC-1	pancreas:	n/a
31	chr9:10966083-10966133	BE2_C	brain:	n/a
32	chr9:10966083-10966133	BJ	skin:	n/a
33	chr9:10966083-10966133	AG04450	lung:	fetal
34	chr9:10966083-10966133	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:10966083-10966133	Caco-2	colon:	n/a
36	chr9:10966083-10966133	HIPEpiC	eye:	n/a
37	chr9:10966083-10966133	ovcar-3	ovarian:	n/a
38	chr9:10966083-10966133	SKMC	muscle:	n/a
39	chr9:10966083-10966133	LNCaP	prostate:	n/a
40	chr9:10966083-10966133	T-47D	breast:	n/a
41	chr9:10966083-10966133	HRE	kidney:	n/a
42	chr9:10966083-10966133	PFSK-1	brain:	n/a
43	chr9:10966083-10966133	MCF-7	breast:	n/a
44	chr9:10966083-10966133	HMEC	breast:	n/a
45	chr9:10966083-10966133	U87	brain:	n/a
46	chr9:10966083-10966133	HepG2	liver:	n/a
47	chr9:10966083-10966133	AG09309	skin:	n/a
48	chr9:10966083-10966133	HNPCEpiC	eye:	n/a
49	chr9:10966083-10966133	Hepatocyte	liver:	n/a
50	chr9:10966083-10966133	HL-60	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
2	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
3	chr9:10799917..10802612-chr9:10809081..10811192,2	K562	blood:
4	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
5	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
6	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
7	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
8	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
9	chr9:10855600..10856394-chr9:12425953..12426703,2	MCF-7	breast:
10	chr9:10800011..10802927-chr9:10803312..10805681,2	K562	blood:
11	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
12	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
13	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
14	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
15	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
16	chr1:210502189..210502757-chr9:11220602..11221102,2	HCT-116	colon:
17	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
18	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
19	chr9:10656522..10658673-chr9:10675612..10678102,2	K562	blood:
20	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
21	chr11:13082457..13083259-chr9:11319197..11319700,2	MCF-7	breast:
22	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
23	chr9:11115862..11118704-chr9:11119627..11122004,2	MCF-7	breast:
24	chr9:10800011..10802927-chr9:10803312..10805681,2	K562	blood:
25	chr9:10656522..10658673-chr9:10675612..10678102,2	K562	blood:
26	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
27	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
28	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
29	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
30	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
31	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
32	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
33	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
34	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
35	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
36	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
37	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
38	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
39	chr9:11115862..11118704-chr9:11119627..11122004,2	MCF-7	breast:
40	chr16:12541131..12541857-chr9:11173536..11174397,2	MCF-7	breast:
41	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
42	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
43	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:
44	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
45	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
46	chr9:10799917..10802612-chr9:10809081..10811192,2	K562	blood:
47	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:
48	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:
49	chr9:10697506..10699235-chr9:10701323..10703741,2	K562	blood:
50	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-3	chr9:11172260-11172372	XLOC_007645
2	lnc-TYRP1-1	chr9:11325743-11325750	XLOC_007282
3	lnc-PTPRD-2	chr9:11108072-11109984	XLOC_007644
4	lnc-PTPRD-4	chr9:11275314-11275536	XLOC_007646
5	lnc-PTPRD-3	chr9:11143876-11144029	XLOC_007645
6	lnc-PTPRD-9	chr9:11265314-11265536	NONHSAT130211
7	lnc-PTPRD-7	chr9:10948366-10948481	NONHSAT130207
8	lnc-PTPRD-7	chr9:10958410-10958540	NONHSAT130207
9	lnc-PTPRD-4	chr9:11276253-11276314	XLOC_007646
10	lnc-TYRP1-1	chr9:11313363-11313595	XLOC_007282
11	lnc-PTPRD-2	chr9:11097567-11097597	XLOC_007644
12	lnc-TYRP1-2	chr9:11277589-11277655	XLOC_007281
13	lnc-TYRP1-2	chr9:11277792-11277964	XLOC_007281
14	lnc-PTPRD-3	chr9:11159533-11159565	XLOC_007645
15	lnc-PTPRD-3	chr9:11194276-11194381	XLOC_007645
16	lnc-PTPRD-9	chr9:11266253-11266314	NONHSAT130211

No data

Variant related genes	Relation type
ENSG00000270372	TF binding region
ENSG00000230365	TF binding region
ENSG00000227138	TF binding region
ENSG00000234146	TF binding region
IMP3P1	TF binding region
ENSG00000270372	CpG island
ENSG00000230365	CpG island
ENSG00000227138	CpG island
ENSG00000234146	CpG island
IMP3P1	CpG island
ENSG00000054392	chromatin interactions
CSRNP3	miRNA target sites
CSNK1G2	miRNA target sites

Extended variants
information (count: 11713 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:11713 , 50 per page) page: 1 2 3 4 5 6 7 ... 235

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16926225	chr9:10648878-10648879	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541172758	chr9:10648890-10648891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1923439	chr9:10648898-10648899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533244629	chr9:10648901-10648902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142009666	chr9:10648927-10648928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563321729	chr9:10648941-10648942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571188269	chr9:10648968-10648969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376801422	chr9:10648993-10648994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529581736	chr9:10649043-10649044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536984164	chr9:10649064-10649065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556729189	chr9:10649068-10649069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549617923	chr9:10649089-10649090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538892842	chr9:10649093-10649094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566149831	chr9:10649105-10649106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528637466	chr9:10649152-10649153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551999063	chr9:10649180-10649181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557413679	chr9:10649191-10649192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570599231	chr9:10649199-10649200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539522764	chr9:10649299-10649300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1322303	chr9:10649309-10649310	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs569602375	chr9:10649369-10649370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535396515	chr9:10649376-10649377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1998341	chr9:10649385-10649386	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs572248457	chr9:10649496-10649497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114364399	chr9:10649595-10649596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557514659	chr9:10649616-10649617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2208707	chr9:10649660-10649661	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs78188559	chr9:10649751-10649752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563356738	chr9:10649807-10649808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529247146	chr9:10649814-10649815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542955120	chr9:10649870-10649871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62537582	chr9:10649873-10649874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74906141	chr9:10649911-10649912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552035913	chr9:10649968-10649969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551306799	chr9:10661283-10661284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145594605	chr9:10661296-10661297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530916852	chr9:10661299-10661300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186720860	chr9:10661300-10661301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10756088	chr9:10661370-10661371	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs114556135	chr9:10661377-10661378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546995763	chr9:10661386-10661387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567073641	chr9:10661389-10661390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539286011	chr9:10661392-10661393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558895106	chr9:10661401-10661402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191557763	chr9:10661407-10661408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370095879	chr9:10661410-10661411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556682206	chr9:10661449-10661450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148485046	chr9:10661458-10661459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10809149	chr9:10661479-10661480	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs542240504	chr9:10661528-10661529	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
abnormal development	18461090	CNVD
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
Renal cell carcinoma	21215367	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Melanoma	20688739	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Glioma	20126413	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10648800-10650000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr9:10661200-10662200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:10661400-10662400	Enhancers	Fetal Heart	heart
4	chr9:10673800-10675200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:10674400-10675200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr9:10674400-10675200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr9:10674800-10675200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr9:10675800-10676000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:10675800-10676000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
10	chr9:10676000-10677600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:10678400-10679000	Enhancers	NH-A	brain
12	chr9:10685600-10686400	Enhancers	Placenta Amnion	Placenta Amnion
13	chr9:10686600-10687800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr9:10687200-10688000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr9:10687400-10688000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr9:10687400-10688000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr9:10696200-10697200	Enhancers	HepG2	liver
18	chr9:10699600-10700600	Enhancers	Stomach Mucosa	stomach
19	chr9:10700400-10700800	Enhancers	NH-A	brain
20	chr9:10700600-10701000	Weak transcription	Stomach Mucosa	stomach
21	chr9:10701000-10701600	Enhancers	Stomach Mucosa	stomach
22	chr9:10701600-10704400	Weak transcription	Stomach Mucosa	stomach
23	chr9:10704400-10707400	Enhancers	Stomach Mucosa	stomach
24	chr9:10704600-10705000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr9:10704600-10705000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr9:10704600-10705200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr9:10704600-10707600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr9:10729200-10729600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr9:10729400-10729800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr9:10749000-10749600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:10761800-10762400	Enhancers	Fetal Brain Male	brain
32	chr9:10762200-10764800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:10762400-10764200	Weak transcription	Fetal Brain Male	brain
34	chr9:10762600-10763000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr9:10764200-10765200	Enhancers	Fetal Brain Male	brain
36	chr9:10773000-10775000	Enhancers	Fetal Brain Female	brain
37	chr9:10773200-10774400	Enhancers	Fetal Lung	lung
38	chr9:10773400-10773800	Enhancers	Fetal Brain Male	brain
39	chr9:10775600-10775800	Enhancers	Fetal Brain Male	brain
40	chr9:10790200-10790600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:10790400-10791600	ZNF genes & repeats	Pancreas	Pancrea
42	chr9:10804200-10804800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:10804400-10804800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr9:10804600-10805000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr9:10804600-10805000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:10804800-10806400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:10805000-10806800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr9:10806400-10807200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:10806600-10806800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr9:10806800-10807200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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