Variant report

Variant	nsv892301
Chromosome Location	chr9:9971050-10144584
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	chr9:10045783-10045920	HepG2	liver:	n/a	n/a
2	BACH1	chr9:10008391-10008587	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:10059064-10059467	MCF-7	breast:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
4	CEBPB	chr9:10059025-10059505	ECC-1	luminal epithelium:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
5	CEBPB	chr9:10000095-10000401	IMR90	lung:	n/a	chr9:10000229-10000240
6	CEBPB	chr9:9983589-9983789	A549	lung:	n/a	n/a
7	CEBPB	chr9:10059065-10059560	IMR90	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
8	CEBPB	chr9:10101585-10101907	IMR90	lung:	n/a	chr9:10101728-10101739 chr9:10101730-10101739 chr9:10101730-10101739 chr9:10101729-10101740 chr9:10101730-10101739 chr9:10101728-10101741 chr9:10101730-10101739
9	CEBPB	chr9:10059096-10059483	Hela-S3	cervix:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
10	CEBPB	chr9:10059095-10059482	A549	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
11	CEBPB	chr9:10101598-10101883	A549	lung:	n/a	chr9:10101728-10101739 chr9:10101730-10101739 chr9:10101730-10101739 chr9:10101729-10101740 chr9:10101730-10101739 chr9:10101728-10101741 chr9:10101730-10101739
12	CEBPB	chr9:9975513-9975767	HepG2	liver:	n/a	chr9:9975624-9975635
13	CEBPB	chr9:10059029-10059551	ECC-1	luminal epithelium:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
14	CEBPB	chr9:10059095-10059476	K562	blood:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
15	CEBPB	chr9:10059013-10059547	A549	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
16	CEBPB	chr9:10059043-10059532	A549	lung:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
17	CEBPB	chr9:10058985-10059505	MCF-7	breast:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
18	CEBPB	chr9:10050102-10050399	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:10059167-10059392	HepG2	liver:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
20	CEBPB	chr9:10000119-10000362	A549	lung:	n/a	chr9:10000229-10000240
21	CEBPB	chr9:9982174-9982447	IMR90	lung:	n/a	chr9:9982310-9982323
22	CEBPB	chr9:10059113-10059428	HepG2	liver:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
23	CEBPB	chr9:10073607-10073661	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:10000093-10000360	HepG2	liver:	n/a	chr9:10000229-10000240
25	CEBPB	chr9:10101562-10101892	HepG2	liver:	n/a	chr9:10101728-10101739 chr9:10101730-10101739 chr9:10101730-10101739 chr9:10101729-10101740 chr9:10101730-10101739 chr9:10101728-10101741 chr9:10101730-10101739
26	CEBPB	chr9:10125227-10125411	HepG2	liver:	n/a	chr9:10125267-10125278
27	CEBPB	chr9:10059096-10059479	HepG2	liver:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
28	CEBPB	chr9:10126127-10126248	HepG2	liver:	n/a	chr9:10126189-10126200 chr9:10126147-10126158
29	CEBPB	chr9:10130155-10130709	IMR90	lung:	n/a	chr9:10130521-10130533
30	CEBPB	chr9:10000141-10000327	H1-hESC	embryonic stem cell:	n/a	chr9:10000229-10000240
31	CEBPB	chr9:9997246-9997453	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr9:10059063-10059490	H1-hESC	embryonic stem cell:	n/a	chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059283-10059292 chr9:10059281-10059294 chr9:10059282-10059293
33	CHD2	chr9:10008242-10008651	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr9:10045680-10045830	HAc	cerebellar:	n/a	n/a
35	CTCF	chr9:10026520-10026670	GM12872	blood:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
36	CTCF	chr9:10060520-10060670	HCM	heart:	n/a	n/a
37	CTCF	chr9:10060400-10060550	K562	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
38	CTCF	chr9:10060420-10060570	AG09309	skin:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
39	CTCF	chr9:10026540-10026690	GM12872	blood:	n/a	chr9:10026618-10026634 chr9:10026619-10026640
40	CTCF	chr9:10022144-10022258	GM20000	blood:	n/a	n/a
41	CTCF	chr9:10060380-10060530	GM12801	blood:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521
42	CTCF	chr9:9998560-9998710	AG04449	skin:	n/a	n/a
43	CTCF	chr9:9998500-9998650	Caco-2	colon:	n/a	n/a
44	CTCF	chr9:10060367-10060658	HUVEC	blood vessel:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
45	CTCF	chr9:10060960-10061110	AG10803	skin:	n/a	n/a
46	CTCF	chr9:9998560-9998710	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr9:10060440-10060590	Caco-2	colon:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
48	CTCF	chr9:10060520-10060670	HVMF	connective:	n/a	n/a
49	CTCF	chr9:10060440-10060590	AG04450	lung:	n/a	chr9:10060508-10060526 chr9:10060509-10060525 chr9:10060511-10060524 chr9:10060513-10060521 chr9:10060510-10060531
50	CTCF	chr9:9998580-9998730	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9998791-9998841	Hepatocyte	liver:	n/a
2	chr9:9998791-9998841	MCF-7	breast:	n/a
3	chr9:9998791-9998841	BJ	skin:	n/a
4	chr9:9998791-9998841	HAEpiC	amniotic membrane:	n/a
5	chr9:9998791-9998841	T-47D	breast:	n/a
6	chr9:9998791-9998841	ProgFib	skin:	n/a
7	chr9:9998791-9998841	AG04450	lung:	fetal
8	chr9:9998791-9998841	GM19239	blood:	n/a
9	chr9:9998791-9998841	AG04449	skin:	fetal
10	chr9:9998791-9998841	ovcar-3	ovarian:	n/a
11	chr9:9998791-9998841	MCF10A-Er-Src	breast:	n/a
12	chr9:9998791-9998841	BE2_C	brain:	n/a
13	chr9:9998791-9998841	HRPEpiC	eye:	n/a
14	chr9:9998791-9998841	PFSK-1	brain:	n/a
15	chr9:9998791-9998841	IMR90	lung:	fetal
16	chr9:9998791-9998841	AG10803	skin:	n/a
17	chr9:9998791-9998841	U87	brain:	n/a
18	chr9:9998791-9998841	GM12892	blood:	n/a
19	chr9:9998791-9998841	GM12891	blood:	n/a
20	chr9:9998791-9998841	CMK	blood:	n/a
21	chr9:9998791-9998841	HepG2	liver:	n/a
22	chr9:9998791-9998841	Hela-S3	cervix:	n/a
23	chr9:9998791-9998841	H1-hESC	embryonic stem cell:	embryo
24	chr9:9998791-9998841	A549	lung:	n/a
25	chr9:9998791-9998841	ECC-1	luminal epithelium:	n/a
26	chr9:9998791-9998841	RPTEC	kidney:	n/a
27	chr9:9998791-9998841	HMEC	breast:	n/a
28	chr9:9998791-9998841	SK-N-MC	brain:	n/a
29	chr9:9998791-9998841	GM12878	blood:	n/a
30	chr9:9998791-9998841	NH-A	brain:	n/a
31	chr9:9998791-9998841	GM06990	blood:	n/a
32	chr9:9998791-9998841	NT2-D1	testis:	n/a
33	chr9:9998791-9998841	HEK293	kidney:	embryo
34	chr9:9998791-9998841	NHBE	bronchial:	n/a
35	chr9:9998791-9998841	HRCEpiC	kidney:	n/a
36	chr9:9998791-9998841	HCF	heart:	n/a
37	chr9:9998791-9998841	HNPCEpiC	eye:	n/a
38	chr9:9998791-9998841	AoSMC	blood vessel:	n/a
39	chr9:9998791-9998841	Caco-2	colon:	n/a
40	chr9:9998791-9998841	AG09309	skin:	n/a
41	chr9:9998791-9998841	SK-N-SH	brain:	n/a
42	chr9:9998791-9998841	PANC-1	pancreas:	n/a
43	chr9:9998791-9998841	Jurkat	blood:	n/a
44	chr9:9998791-9998841	HRE	kidney:	n/a
45	chr9:9998791-9998841	AG09319	gingival:	n/a
46	chr9:9998791-9998841	SKMC	muscle:	n/a
47	chr9:9998791-9998841	HIPEpiC	eye:	n/a
48	chr9:9998791-9998841	HCM	heart:	n/a
49	chr9:9998791-9998841	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:9998791-9998841	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10045409..10046174-chr9:10268540..10269128,2	MCF-7	breast:
2	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:
3	chr9:10053198..10055670-chr9:10065089..10066974,2	K562	blood:
4	chr9:10060352..10060896-chr9:10268535..10269397,2	MCF-7	breast:

Variant related genes	Relation type
PTPRD	TF binding region
PTPRD	CpG island

Extended variants
information (count: 5595 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:5595 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10114140	chr9:9971050-9971051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541143654	chr9:9971068-9971069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116029594	chr9:9971076-9971077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148869080	chr9:9971137-9971138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376535177	chr9:9971160-9971161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181954077	chr9:9971164-9971165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377346764	chr9:9971169-9971170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185131415	chr9:9971184-9971185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529286235	chr9:9971187-9971188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556995654	chr9:9971202-9971203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115753955	chr9:9971214-9971215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10123237	chr9:9971262-9971263	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs528527834	chr9:9971269-9971270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371964661	chr9:9971280-9971281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551861052	chr9:9971304-9971305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375671946	chr9:9971331-9971332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571738305	chr9:9971357-9971358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546056412	chr9:9971369-9971370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143558286	chr9:9971409-9971410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10978143	chr9:9971410-9971411	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs114699166	chr9:9971427-9971428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374577353	chr9:9971437-9971438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148314023	chr9:9971463-9971464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190038172	chr9:9971491-9971492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571712327	chr9:9971543-9971544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117037821	chr9:9971557-9971558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557876577	chr9:9971559-9971560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577760687	chr9:9971564-9971565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552267908	chr9:9971642-9971643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561279239	chr9:9971719-9971720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530287032	chr9:9971721-9971722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73643837	chr9:9971799-9971800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13290231	chr9:9971805-9971806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570591244	chr9:9971826-9971827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114224610	chr9:9971833-9971834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542130052	chr9:9971910-9971911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141646429	chr9:9971929-9971930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147034790	chr9:9971930-9971931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559740891	chr9:9971952-9971953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555669460	chr9:9972017-9972018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376198645	chr9:9972020-9972021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538830827	chr9:9972040-9972041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528524943	chr9:9972057-9972058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10978144	chr9:9972069-9972070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183239311	chr9:9972076-9972077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186497148	chr9:9972123-9972124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530995890	chr9:9972137-9972138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377715450	chr9:9972145-9972146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572229663	chr9:9972150-9972151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550726882	chr9:9972151-9972152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	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
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21611746	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Glioma	20126413	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9970000-9972800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:9972800-9973000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:9972800-9973600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr9:9973200-9973600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr9:9989600-9989800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:9989800-9990000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:9989800-10000400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:9990000-9999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:9990200-9990600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:9994200-9994400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:9994400-9995000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr9:9995000-9995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:9995000-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:9995200-9995800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:9995200-9996200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:9995200-9998000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr9:9995200-9998200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr9:9995200-9999200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr9:9995200-9999200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr9:9995200-9999400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr9:9995200-10001000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:9995400-9995600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr9:9995400-9995600	Enhancers	H9 Cell Line	embryonic stem cell
24	chr9:9995400-9995600	Enhancers	Primary hematopoietic stem cells	blood
25	chr9:9995400-9995800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:9995400-9997200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr9:9995600-9996200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr9:9995600-9996400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr9:9995600-9996400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr9:9995600-9997200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:9995800-9996400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr9:9996200-9997600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:9996200-9999000	Enhancers	Primary hematopoietic stem cells	blood
34	chr9:9996400-9996600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr9:9996400-9996600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr9:9996400-9996800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr9:9996400-9996800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:9996400-9996800	Enhancers	Stomach Mucosa	stomach
39	chr9:9996400-9997000	Enhancers	Fetal Kidney	kidney
40	chr9:9996400-9997200	Enhancers	HUVEC	blood vessel
41	chr9:9996600-9997400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr9:9996600-9997400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr9:9996800-9998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr9:9996800-9999200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr9:9997200-9997600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr9:9997200-9998200	Weak transcription	HUVEC	blood vessel
47	chr9:9997200-9999000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:9997200-9999200	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr9:9997400-9997800	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr9:9997400-9998600	Enhancers	H1 Cell Line	embryonic stem cell

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