Variant report

Variant	nsv1021035
Chromosome Location	chr9:10755356-11281192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:948)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:948 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr9:10910431-10910585	K562	blood:	n/a	n/a
7	BACH1	chr9:11067007-11067064	K562	blood:	n/a	n/a
8	BACH1	chr9:11016111-11016284	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr9:11038049-11038208	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr9:10921715-10922010	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr9:11064885-11065303	K562	blood:	n/a	n/a
12	BHLHE40	chr9:11064998-11065193	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:11065067-11065094	GM12878	blood:	n/a	n/a
14	BRCA1	chr9:11064953-11065285	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr9:11272473-11272479	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:11064529-11064729	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr9:11064870-11065315	K562	blood:	n/a	n/a
18	CBX3	chr9:11269115-11269340	K562	blood:	n/a	n/a
19	CEBPB	chr9:11221350-11221590	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:10937715-10937998	HepG2	liver:	n/a	chr9:10937875-10937886
21	CEBPB	chr9:11084605-11084942	HepG2	liver:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
22	CEBPB	chr9:10870850-10871156	HepG2	liver:	n/a	chr9:10870983-10870994
23	CEBPB	chr9:10864332-10864582	A549	lung:	n/a	chr9:10864432-10864449 chr9:10864433-10864444 chr9:10864433-10864446 chr9:10864434-10864445 chr9:10864480-10864491
24	CEBPB	chr9:10864356-10864613	Hela-S3	cervix:	n/a	chr9:10864432-10864449 chr9:10864433-10864444 chr9:10864433-10864446 chr9:10864434-10864445 chr9:10864480-10864491
25	CEBPB	chr9:10838394-10838591	HepG2	liver:	n/a	chr9:10838508-10838519
26	CEBPB	chr9:10921657-10922056	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:10929200-10929413	HepG2	liver:	n/a	chr9:10929234-10929247 chr9:10929234-10929245 chr9:10929234-10929247 chr9:10929293-10929304
28	CEBPB	chr9:10997736-10998005	A549	lung:	n/a	chr9:10997888-10997899
29	CEBPB	chr9:11143390-11143713	IMR90	lung:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
30	CEBPB	chr9:10957899-10958248	IMR90	lung:	n/a	chr9:10958059-10958070
31	CEBPB	chr9:11267017-11267301	K562	blood:	n/a	chr9:11267135-11267146
32	CEBPB	chr9:10920298-10920309	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:10978428-10978694	HepG2	liver:	n/a	chr9:10978574-10978585
34	CEBPB	chr9:11143432-11143632	H1-hESC	embryonic stem cell:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
35	CEBPB	chr9:10928603-10928846	HepG2	liver:	n/a	chr9:10928719-10928730
36	CEBPB	chr9:11217166-11217491	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:11143392-11143656	K562	blood:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
38	CEBPB	chr9:11257560-11257807	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:11084639-11084926	A549	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
40	CEBPB	chr9:10937740-10938007	IMR90	lung:	n/a	chr9:10937875-10937886
41	CEBPB	chr9:10800986-10801148	HepG2	liver:	n/a	chr9:10801096-10801107
42	CEBPB	chr9:11266996-11267317	IMR90	lung:	n/a	chr9:11267135-11267146
43	CEBPB	chr9:11049857-11050082	K562	blood:	n/a	n/a
44	CEBPB	chr9:11073722-11074080	A549	lung:	n/a	chr9:11073895-11073908 chr9:11073895-11073906
45	CEBPB	chr9:10864349-10864630	HepG2	liver:	n/a	chr9:10864432-10864449 chr9:10864433-10864444 chr9:10864433-10864446 chr9:10864434-10864445 chr9:10864480-10864491
46	CEBPB	chr9:11143371-11143702	HepG2	liver:	n/a	chr9:11143522-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143524-11143533 chr9:11143523-11143534 chr9:11143524-11143533
47	CEBPB	chr9:10789715-10790204	HepG2	liver:	n/a	chr9:10790076-10790087
48	CEBPB	chr9:11084602-11084944	IMR90	lung:	n/a	chr9:11084785-11084796 chr9:11084784-11084797 chr9:11084784-11084795
49	CEBPB	chr9:10957932-10958241	H1-hESC	embryonic stem cell:	n/a	chr9:10958059-10958070
50	CEBPB	chr9:11258136-11258368	H1-hESC	embryonic stem cell:	n/a	chr9:11258233-11258244

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:10966083-10966133	ProgFib	skin:	n/a
2	chr9:10966083-10966133	PrEC	prostate:	n/a
3	chr9:10966083-10966133	AG09319	gingival:	n/a
4	chr9:10966083-10966133	H1-hESC	embryonic stem cell:	embryo
5	chr9:10966083-10966133	SK-N-MC	brain:	n/a
6	chr9:10966083-10966133	AG09309	skin:	n/a
7	chr9:10966083-10966133	HCPEpiC	choroid plexus:	n/a
8	chr9:10966083-10966133	NHBE	bronchial:	n/a
9	chr9:10966083-10966133	HEK293	kidney:	embryo
10	chr9:10966083-10966133	HRE	kidney:	n/a
11	chr9:10966083-10966133	RPTEC	kidney:	n/a
12	chr9:10966083-10966133	HPAEpiC	pulmonary alveolar:	n/a
13	chr9:10966083-10966133	NB4	blood:	n/a
14	chr9:10966083-10966133	HAEpiC	amniotic membrane:	n/a
15	chr9:10966083-10966133	MCF10A-Er-Src	breast:	n/a
16	chr9:10966083-10966133	HCF	heart:	n/a
17	chr9:10966083-10966133	SAEC	small airway:	n/a
18	chr9:10966083-10966133	K562	blood:	n/a
19	chr9:10966083-10966133	Hepatocyte	liver:	n/a
20	chr9:10966083-10966133	HRCEpiC	kidney:	n/a
21	chr9:10966083-10966133	ECC-1	luminal epithelium:	n/a
22	chr9:10966083-10966133	GM19239	blood:	n/a
23	chr9:10966083-10966133	GM12878	blood:	n/a
24	chr9:10966083-10966133	SK-N-SH	brain:	n/a
25	chr9:10966083-10966133	A549	lung:	n/a
26	chr9:10966083-10966133	HNPCEpiC	eye:	n/a
27	chr9:10966083-10966133	HEEpiC	esophagus:	n/a
28	chr9:10966083-10966133	HRPEpiC	eye:	n/a
29	chr9:10966083-10966133	BJ	skin:	n/a
30	chr9:10966083-10966133	NHDF-neo	bronchial:	n/a
31	chr9:10966083-10966133	HMEC	breast:	n/a
32	chr9:10966083-10966133	HCM	heart:	n/a
33	chr9:10966083-10966133	NT2-D1	testis:	n/a
34	chr9:10966083-10966133	HepG2	liver:	n/a
35	chr9:10966083-10966133	PFSK-1	brain:	n/a
36	chr9:10966083-10966133	AG04449	skin:	fetal
37	chr9:10966083-10966133	ovcar-3	ovarian:	n/a
38	chr9:10966083-10966133	HIPEpiC	eye:	n/a
39	chr9:10966083-10966133	Caco-2	colon:	n/a
40	chr9:10966083-10966133	Jurkat	blood:	n/a
41	chr9:10966083-10966133	CMK	blood:	n/a
42	chr9:10966083-10966133	GM12892	blood:	n/a
43	chr9:10966083-10966133	AoSMC	blood vessel:	n/a
44	chr9:10966083-10966133	MCF-7	breast:	n/a
45	chr9:10966083-10966133	T-47D	breast:	n/a
46	chr9:10966083-10966133	BE2_C	brain:	n/a
47	chr9:10966083-10966133	PANC-1	pancreas:	n/a
48	chr9:10966083-10966133	LNCaP	prostate:	n/a
49	chr9:10966083-10966133	AG10803	skin:	n/a
50	chr9:10966083-10966133	SKMC	muscle:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:10799917..10802612-chr9:10809081..10811192,2	K562	blood:
2	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
3	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
4	chr9:10855600..10856394-chr9:12425953..12426703,2	MCF-7	breast:
5	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
6	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
7	chr1:210502189..210502757-chr9:11220602..11221102,2	HCT-116	colon:
8	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:
9	chr17:59389836..59390496-chr9:10867919..10868419,2	MCF-7	breast:
10	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
11	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
12	chr9:11018319..11020122-chr9:11028284..11030426,2	K562	blood:
13	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:
14	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
15	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
16	chr9:11115862..11118704-chr9:11119627..11122004,2	MCF-7	breast:
17	chr9:11115862..11118704-chr9:11119627..11122004,2	MCF-7	breast:
18	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
19	chr9:11056159..11057837-chr9:11062194..11064646,2	K562	blood:
20	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:
21	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
22	chr9:11216192..11218001-chr9:11219669..11221559,2	K562	blood:
23	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
24	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
25	chr9:11026162..11028762-chr9:11041183..11043715,2	K562	blood:
26	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
27	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
28	chr9:11049044..11051208-chr9:11053146..11055450,2	K562	blood:
29	chr9:11039996..11042346-chr9:11065271..11066776,2	K562	blood:
30	chr9:11052013..11055648-chr9:11062078..11065783,4	K562	blood:
31	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
32	chr9:11063987..11066726-chr9:11070793..11073075,2	MCF-7	breast:
33	chr9:10799917..10802612-chr9:10809081..10811192,2	K562	blood:
34	chr9:11059291..11061789-chr9:11063668..11065240,2	MCF-7	breast:
35	chr9:10800011..10802927-chr9:10803312..10805681,2	K562	blood:
36	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
37	chr16:12541131..12541857-chr9:11173536..11174397,2	MCF-7	breast:
38	chr9:11044597..11046205-chr9:11057945..11060223,2	MCF-7	breast:
39	chr9:11053156..11054741-chr9:11055812..11058059,2	K562	blood:
40	chr9:11056337..11059587-chr9:11061284..11064646,4	K562	blood:
41	chr9:11047509..11049109-chr9:11061184..11063575,2	MCF-7	breast:
42	chr9:11047082..11049411-chr9:11061377..11064321,2	K562	blood:
43	chr9:11064416..11066663-chr9:11091382..11093294,2	MCF-7	breast:
44	chr9:10800011..10802927-chr9:10803312..10805681,2	K562	blood:
45	chr9:11051115..11054715-chr9:11062496..11065504,4	K562	blood:

(count:14 , 50 per page) page: 1

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

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
CSNK1G2	miRNA target sites
CSRNP3	miRNA target sites

Extended variants
information (count: 8170 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:8170 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185869437	chr9:10761807-10761808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560898958	chr9:10761831-10761832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530261637	chr9:10761868-10761869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572306175	chr9:10761869-10761870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568505150	chr9:10761873-10761874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560125533	chr9:10761891-10761892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142673573	chr9:10761898-10761899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs398113237	chr9:10761905-10761906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532328170	chr9:10761930-10761931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538623573	chr9:10761955-10761956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117395190	chr9:10761963-10761964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12554421	chr9:10762022-10762023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76189892	chr9:10762042-10762043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559304198	chr9:10762063-10762064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531886978	chr9:10762064-10762065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374043417	chr9:10762101-10762102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548807997	chr9:10762106-10762107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568550581	chr9:10762113-10762114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536351516	chr9:10762117-10762118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199708622	chr9:10762120-10762121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553064935	chr9:10762140-10762141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190193321	chr9:10762163-10762164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538610405	chr9:10762215-10762216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569526258	chr9:10762241-10762242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117195878	chr9:10762253-10762254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540938081	chr9:10762256-10762257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536506970	chr9:10762257-10762258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576438139	chr9:10762276-10762277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575643191	chr9:10762306-10762307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554873278	chr9:10762324-10762325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183139629	chr9:10762326-10762327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574498475	chr9:10762380-10762381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540728779	chr9:10762397-10762398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560176632	chr9:10762407-10762408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532389085	chr9:10762420-10762421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12377865	chr9:10762438-10762439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185990108	chr9:10762451-10762452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149303935	chr9:10762455-10762456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532080661	chr9:10762476-10762477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375949379	chr9:10762498-10762499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548553993	chr9:10762523-10762524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568649438	chr9:10762551-10762552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540344519	chr9:10762564-10762565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540407705	chr9:10762568-10762569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148580214	chr9:10762600-10762601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566599506	chr9:10762617-10762618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192363429	chr9:10762623-10762624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10122605	chr9:10762689-10762690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141956905	chr9:10762710-10762711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538144783	chr9:10762726-10762727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Bipolar disorder	19114987	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10761800-10762400	Enhancers	Fetal Brain Male	brain
2	chr9:10762200-10764800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:10762400-10764200	Weak transcription	Fetal Brain Male	brain
4	chr9:10762600-10763000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:10764200-10765200	Enhancers	Fetal Brain Male	brain
6	chr9:10773000-10775000	Enhancers	Fetal Brain Female	brain
7	chr9:10773200-10774400	Enhancers	Fetal Lung	lung
8	chr9:10773400-10773800	Enhancers	Fetal Brain Male	brain
9	chr9:10775600-10775800	Enhancers	Fetal Brain Male	brain
10	chr9:10790200-10790600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:10790400-10791600	ZNF genes & repeats	Pancreas	Pancrea
12	chr9:10804200-10804800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:10804400-10804800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr9:10804600-10805000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:10804600-10805000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr9:10804800-10806400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:10805000-10806800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr9:10806400-10807200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:10806600-10806800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:10806800-10807200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:10807000-10807400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:10807200-10808000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:10808000-10809000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:10808400-10808800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:10812600-10813000	Enhancers	Fetal Brain Male	brain
26	chr9:10829800-10830000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:10829800-10830200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:10833400-10834200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:10836000-10836400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr9:10836200-10836400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:10869600-10870200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr9:10869600-10870200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:10869600-10870400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr9:10869800-10870400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr9:10872000-10872200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr9:10872400-10873000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:10873000-10876400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:10875000-10877200	Enhancers	HUVEC	blood vessel
39	chr9:10875200-10876400	Enhancers	Hela-S3	cervix
40	chr9:10875600-10877000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:10875800-10877000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr9:10876000-10876200	Enhancers	Stomach Mucosa	stomach
43	chr9:10876000-10876800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr9:10876200-10877000	Weak transcription	Stomach Mucosa	stomach
45	chr9:10876400-10876600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:10876400-10876800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:10877000-10878200	Enhancers	Stomach Mucosa	stomach
48	chr9:10881400-10882400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr9:10887200-10887400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
50	chr9:10887400-10888600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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