Variant report

Variant	nsv521363
Chromosome Location	chr9:14566406-14691897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:965)
CpG islands
(count:184)
Chromatin interactive
region (count:35)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14616366-14616729	K562	blood:	n/a	n/a
2	ARID3A	chr9:14652772-14653234	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14616384-14616695	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:14661451-14661789	K562	blood:	n/a	n/a
5	ATF1	chr9:14661502-14661775	K562	blood:	n/a	n/a
6	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
7	ATF2	chr9:14585562-14586344	GM12878	blood:	n/a	n/a
8	ATF2	chr9:14585524-14586203	GM12878	blood:	n/a	n/a
9	BACH1	chr9:14573620-14573628	K562	blood:	n/a	n/a
10	BATF	chr9:14585675-14586118	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:14585726-14586068	GM12878	blood:	n/a	chr9:14585907-14585916
12	BCL11A	chr9:14585612-14586175	GM12878	blood:	n/a	chr9:14585907-14585916
13	BCL3	chr9:14585642-14586081	GM12878	blood:	n/a	chr9:14585907-14585916
14	BCLAF1	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
15	BCLAF1	chr9:14585603-14586186	GM12878	blood:	n/a	chr9:14585907-14585916
16	BHLHE40	chr9:14616435-14616720	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:14585516-14586154	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
20	BRCA1	chr9:14652862-14653081	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr9:14593377-14593719	K562	blood:	n/a	n/a
22	CBX3	chr9:14654942-14655330	K562	blood:	n/a	n/a
23	CBX3	chr9:14578017-14578336	K562	blood:	n/a	n/a
24	CBX3	chr9:14654902-14655428	HCT-116	colon:	n/a	n/a
25	CBX3	chr9:14578016-14578324	K562	blood:	n/a	n/a
26	CBX3	chr9:14654938-14655346	K562	blood:	n/a	n/a
27	CBX3	chr9:14654909-14655424	HCT-116	colon:	n/a	n/a
28	CEBPB	chr9:14661506-14661801	K562	blood:	n/a	n/a
29	CEBPB	chr9:14593561-14593669	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:14640433-14640716	A549	lung:	n/a	n/a
31	CEBPB	chr9:14687100-14687489	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:14593410-14593662	K562	blood:	n/a	n/a
33	CEBPB	chr9:14620535-14620536	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:14626442-14626622	HepG2	liver:	n/a	chr9:14626550-14626561 chr9:14626549-14626562 chr9:14626549-14626560 chr9:14626549-14626562 chr9:14626549-14626562 chr9:14626549-14626560
35	CHD1	chr9:14688156-14688623	GM12878	blood:	n/a	n/a
36	CHD2	chr9:14616421-14616609	GM12878	blood:	n/a	n/a
37	CREB1	chr9:14652817-14653056	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:14616454-14616677	LNCaP	prostate:	n/a	n/a
39	CTCF	chr9:14616460-14616610	MCF-7	breast:	n/a	n/a
40	CTCF	chr9:14653480-14653630	AG04450	lung:	n/a	n/a
41	CTCF	chr9:14652780-14652930	BE2_C	brain:	n/a	n/a
42	CTCF	chr9:14616366-14616700	ECC-1	luminal epithelium:	n/a	n/a
43	CTCF	chr9:14616500-14616650	AG04449	skin:	n/a	n/a
44	CTCF	chr9:14616520-14616670	HRE	kidney:	n/a	n/a
45	CTCF	chr9:14616500-14616650	GM12867	blood:	n/a	n/a
46	CTCF	chr9:14661560-14661710	GM12878	blood:	n/a	chr9:14661642-14661663
47	CTCF	chr9:14652880-14653030	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr9:14616460-14616653	HepG2	liver:	n/a	n/a
49	CTCF	chr9:14616480-14616630	HCT-116	colon:	n/a	n/a
50	CTCF	chr9:14616500-14616650	GM12866	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14643897-14643947	SAEC	small airway:	n/a
2	chr9:14643897-14643947	SAEC	small airway:	n/a
3	chr9:14691289-14691339	HRCEpiC	kidney:	n/a
4	chr9:14690531-14690581	HRE	kidney:	n/a
5	chr9:14691289-14691339	K562	blood:	n/a
6	chr9:14691289-14691339	HL-60	blood:	n/a
7	chr9:14690531-14690581	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:14643897-14643947	HCPEpiC	choroid plexus:	n/a
9	chr9:14690531-14690581	HCM	heart:	n/a
10	chr9:14691289-14691339	GM12878	blood:	n/a
11	chr9:14690531-14690581	BE2_C	brain:	n/a
12	chr9:14690531-14690581	GM12891	blood:	n/a
13	chr9:14643897-14643947	ProgFib	skin:	n/a
14	chr9:14643897-14643947	NT2-D1	testis:	n/a
15	chr9:14690531-14690581	HCT-116	colon:	n/a
16	chr9:14691289-14691339	NT2-D1	testis:	n/a
17	chr9:14691289-14691339	Jurkat	blood:	n/a
18	chr9:14690531-14690581	ovcar-3	ovarian:	n/a
19	chr9:14691289-14691339	HRPEpiC	eye:	n/a
20	chr9:14643897-14643947	H1-hESC	embryonic stem cell:	embryo
21	chr9:14691289-14691339	HEK293	kidney:	embryo
22	chr9:14643897-14643947	AG09309	skin:	n/a
23	chr9:14691289-14691339	HAEpiC	amniotic membrane:	n/a
24	chr9:14691289-14691339	Caco-2	colon:	n/a
25	chr9:14691289-14691339	MCF-7	breast:	n/a
26	chr9:14643897-14643947	GM19239	blood:	n/a
27	chr9:14691289-14691339	MCF10A-Er-Src	breast:	n/a
28	chr9:14691289-14691339	T-47D	breast:	n/a
29	chr9:14643897-14643947	ECC-1	luminal epithelium:	n/a
30	chr9:14643897-14643947	HNPCEpiC	eye:	n/a
31	chr9:14643897-14643947	RPTEC	kidney:	n/a
32	chr9:14690531-14690581	SK-N-SH_RA	brain:	n/a
33	chr9:14691289-14691339	NHBE	bronchial:	n/a
34	chr9:14643897-14643947	Hepatocyte	liver:	n/a
35	chr9:14690531-14690581	CMK	blood:	n/a
36	chr9:14690531-14690581	HCPEpiC	choroid plexus:	n/a
37	chr9:14690531-14690581	IMR90	lung:	fetal
38	chr9:14690531-14690581	HCF	heart:	n/a
39	chr9:14643897-14643947	HCF	heart:	n/a
40	chr9:14643897-14643947	SK-N-SH	brain:	n/a
41	chr9:14643897-14643947	AG10803	skin:	n/a
42	chr9:14643897-14643947	HRCEpiC	kidney:	n/a
43	chr9:14643897-14643947	AG04450	lung:	fetal
44	chr9:14643897-14643947	Jurkat	blood:	n/a
45	chr9:14691289-14691339	HepG2	liver:	n/a
46	chr9:14643897-14643947	K562	blood:	n/a
47	chr9:14643897-14643947	HCT-116	colon:	n/a
48	chr9:14691289-14691339	AoSMC	blood vessel:	n/a
49	chr9:14691289-14691339	GM06990	blood:	n/a
50	chr9:14690531-14690581	AG09309	skin:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
2	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
3	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
4	chr9:14627684..14629345-chr9:14693335..14694855,2	MCF-7	breast:
5	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
6	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
7	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
8	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
9	chr9:14465253..14465899-chr9:14652688..14653342,2	MCF-7	breast:
10	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
11	chr9:14442256..14442845-chr9:14661275..14662107,4	K562	blood:
12	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
13	chr9:14465217..14466121-chr9:14652305..14653436,3	K562	blood:
14	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
15	chr9:14676498..14678344-chr9:14692478..14694843,2	MCF-7	breast:
16	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
17	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
18	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
19	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
20	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
21	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
22	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
23	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
24	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
25	chr9:14442114..14442886-chr9:14652552..14653366,4	MCF-7	breast:
26	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
27	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
28	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
29	chr9:14464938..14465658-chr9:14661578..14662250,2	MCF-7	breast:
30	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
31	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
32	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
33	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
34	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
35	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC21-1	chr9:14611070-14614754	NONHSAT130252
2	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
3	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254
4	lnc-ZDHHC21-4	chr9:14586767-14587324	ENSG00000273399.1
5	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
6	lnc-C9orf146-7	chr9:14588065-14588629	NONHSAT130249
7	lnc-ZDHHC21-3	chr9:14588795-14590063	ENSG00000272871.1
8	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254
9	lnc-C9orf146-8	chr9:14593575-14594198	NONHSAT130250
10	lnc-ZDHHC21-2	chr9:14606167-14606546	NONHSAT130251
11	lnc-C9orf146-7	chr9:14588795-14589277	NONHSAT130249
12	lnc-ZDHHC21-2	chr9:14609848-14609996	NONHSAT130251
13	lnc-C9orf146-7	chr9:14586764-14587315	NONHSAT130249

No data

Variant related genes	Relation type
ENSG00000229029	TF binding region
ENSG00000272871	TF binding region
ENSG00000273399	TF binding region
ENSG00000229029	CpG island
ENSG00000272871	CpG island
ENSG00000273399	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 5810 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5810 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7040652	chr9:14566406-14566407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537613519	chr9:14566416-14566417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187290544	chr9:14566417-14566418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567792566	chr9:14566423-14566424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147175830	chr9:14566429-14566430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533729097	chr9:14566575-14566576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191041895	chr9:14566621-14566622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140073028	chr9:14566649-14566650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548870917	chr9:14566685-14566686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558527258	chr9:14566701-14566702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575120875	chr9:14566705-14566706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145606813	chr9:14566710-14566711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34411204	chr9:14566716-14566717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560734558	chr9:14566790-14566791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574222295	chr9:14566792-14566793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147301430	chr9:14566857-14566858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114797419	chr9:14566858-14566859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568702980	chr9:14566884-14566885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531963958	chr9:14566887-14566888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552073410	chr9:14566934-14566935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117384671	chr9:14566939-14566940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531212176	chr9:14566943-14566944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551222247	chr9:14566951-14566952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567854039	chr9:14566979-14566980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530260042	chr9:14566982-14566983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114080735	chr9:14566986-14566987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181543431	chr9:14567002-14567003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538632060	chr9:14567003-14567004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371806536	chr9:14567013-14567014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201955446	chr9:14567014-14567015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376472829	chr9:14567080-14567081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148787943	chr9:14567116-14567117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114831230	chr9:14567150-14567151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7028531	chr9:14567164-14567165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs7028536	chr9:14567179-14567180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs10115482	chr9:14567207-14567208	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs556258226	chr9:14567210-14567211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553555624	chr9:14567239-14567240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576785169	chr9:14567249-14567250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576389912	chr9:14567253-14567254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7028679	chr9:14567272-14567273	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs139270630	chr9:14567287-14567288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544910765	chr9:14567288-14567289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561477485	chr9:14567311-14567312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185677775	chr9:14567361-14567362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540461850	chr9:14567376-14567377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111825339	chr9:14567383-14567384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10124533	chr9:14567386-14567387	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs532626077	chr9:14567421-14567422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146590337	chr9:14567502-14567503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14564600-14567800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:14565000-14567200	Weak transcription	HepG2	liver
3	chr9:14567000-14568000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr9:14567200-14568000	Enhancers	HepG2	liver
5	chr9:14567800-14568200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:14568000-14568800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:14574400-14575200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr9:14575200-14577400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr9:14575400-14582000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:14575800-14577000	Enhancers	HUVEC	blood vessel
11	chr9:14577000-14577200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:14577000-14577600	Enhancers	Pancreas	Pancrea
13	chr9:14577200-14577400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:14577400-14577600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr9:14577400-14597200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:14577600-14596200	Weak transcription	Pancreas	Pancrea
17	chr9:14582000-14582400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:14582400-14596200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr9:14584400-14584800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr9:14584800-14585200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr9:14585200-14586200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr9:14585200-14587200	Enhancers	GM12878-XiMat	blood
23	chr9:14585200-14589000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:14585400-14586200	Enhancers	Primary B cells from peripheral blood	blood
25	chr9:14585400-14586200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr9:14585400-14586200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr9:14585400-14586400	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr9:14585400-14586400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr9:14585400-14586400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr9:14585400-14586800	Enhancers	Primary T cells from cord blood	blood
31	chr9:14585600-14586000	Enhancers	Primary T cells fromperipheralblood	blood
32	chr9:14585600-14586000	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr9:14585600-14586000	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr9:14585600-14586400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr9:14585800-14586000	Enhancers	Lung	lung
36	chr9:14585800-14586200	Enhancers	Dnd41	blood
37	chr9:14585800-14586400	Enhancers	Brain Germinal Matrix	brain
38	chr9:14585800-14586800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr9:14585800-14598000	Weak transcription	Right Ventricle	heart
40	chr9:14586000-14586200	Enhancers	Fetal Brain Female	brain
41	chr9:14586000-14592000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:14586000-14596200	Weak transcription	Lung	lung
43	chr9:14586000-14597000	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr9:14586200-14595200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr9:14586400-14586600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr9:14586400-14587800	Weak transcription	Aorta	Aorta
47	chr9:14586400-14595800	Weak transcription	Brain Germinal Matrix	brain
48	chr9:14586600-14595200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr9:14586800-14587000	Enhancers	Fetal Brain Female	brain
50	chr9:14586800-14593400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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