Variant report

Variant	esv2752276
Chromosome Location	chr9:11224627-11958106
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	BHLHE40	chr9:11338205-11338405	GM12878	blood:	n/a	n/a
2	BRCA1	chr9:11272473-11272479	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr9:11319527-11319802	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr9:11269115-11269340	K562	blood:	n/a	n/a
5	CEBPB	chr9:11633029-11633280	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:11704304-11704462	HepG2	liver:	n/a	chr9:11704344-11704355
7	CEBPB	chr9:11357845-11358150	IMR90	lung:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
8	CEBPB	chr9:11335919-11336119	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:11294410-11294610	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:11597998-11598356	HepG2	liver:	n/a	chr9:11598247-11598258
11	CEBPB	chr9:11743695-11743965	HepG2	liver:	n/a	chr9:11743800-11743811 chr9:11743833-11743844
12	CEBPB	chr9:11946400-11946627	IMR90	lung:	n/a	chr9:11946481-11946492
13	CEBPB	chr9:11663929-11664298	IMR90	lung:	n/a	chr9:11664111-11664122
14	CEBPB	chr9:11333545-11333604	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr9:11407921-11408170	HepG2	liver:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
16	CEBPB	chr9:11334920-11335231	HepG2	liver:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
17	CEBPB	chr9:11407906-11408170	A549	lung:	n/a	chr9:11408023-11408034 chr9:11408023-11408036
18	CEBPB	chr9:11551626-11551930	HepG2	liver:	n/a	chr9:11551781-11551792
19	CEBPB	chr9:11933909-11934318	Hela-S3	cervix:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
20	CEBPB	chr9:11933929-11934303	IMR90	lung:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
21	CEBPB	chr9:11258112-11258370	A549	lung:	n/a	chr9:11258233-11258244
22	CEBPB	chr9:11434997-11435328	HepG2	liver:	n/a	chr9:11435176-11435187 chr9:11435176-11435189
23	CEBPB	chr9:11664029-11664280	ECC-1	luminal epithelium:	n/a	chr9:11664111-11664122
24	CEBPB	chr9:11663959-11664285	A549	lung:	n/a	chr9:11664111-11664122
25	CEBPB	chr9:11334898-11335195	A549	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
26	CEBPB	chr9:11583943-11584270	HepG2	liver:	n/a	chr9:11584097-11584108
27	CEBPB	chr9:11258136-11258368	H1-hESC	embryonic stem cell:	n/a	chr9:11258233-11258244
28	CEBPB	chr9:11743712-11743936	IMR90	lung:	n/a	chr9:11743800-11743811 chr9:11743833-11743844
29	CEBPB	chr9:11372474-11372712	A549	lung:	n/a	chr9:11372602-11372613
30	CEBPB	chr9:11340773-11341042	HepG2	liver:	n/a	chr9:11340918-11340929
31	CEBPB	chr9:11357865-11358142	HepG2	liver:	n/a	chr9:11357994-11358007 chr9:11357994-11358005 chr9:11357937-11357948
32	CEBPB	chr9:11702572-11702971	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:11633094-11633308	A549	lung:	n/a	n/a
34	CEBPB	chr9:11779927-11780177	A549	lung:	n/a	n/a
35	CEBPB	chr9:11257560-11257807	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:11334919-11335258	IMR90	lung:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
37	CEBPB	chr9:11258134-11258408	HepG2	liver:	n/a	chr9:11258233-11258244
38	CEBPB	chr9:11633011-11633263	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:11614083-11614396	A549	lung:	n/a	chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614243-11614254 chr9:11614245-11614256 chr9:11614243-11614256
40	CEBPB	chr9:11422396-11422505	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:11934067-11934195	HepG2	liver:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
42	CEBPB	chr9:11457829-11458659	H1-hESC	embryonic stem cell:	n/a	chr9:11457991-11458008 chr9:11457994-11458007 chr9:11458637-11458645 chr9:11457994-11458005
43	CEBPB	chr9:11702586-11702895	A549	lung:	n/a	n/a
44	CEBPB	chr9:11946375-11946610	HepG2	liver:	n/a	chr9:11946481-11946492
45	CEBPB	chr9:11614093-11614402	H1-hESC	embryonic stem cell:	n/a	chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614245-11614254 chr9:11614243-11614254 chr9:11614245-11614256 chr9:11614243-11614256
46	CEBPB	chr9:11702581-11702905	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:11334982-11335237	Hela-S3	cervix:	n/a	chr9:11335077-11335088 chr9:11335079-11335090 chr9:11335077-11335090
48	CEBPB	chr9:11603905-11604188	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:11267017-11267301	K562	blood:	n/a	chr9:11267135-11267146
50	CEBPB	chr9:11267004-11267299	HepG2	liver:	n/a	chr9:11267135-11267146

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:11618691-11618741	SK-N-SH_RA	brain:	n/a
2	chr9:11618265-11618315	H1-hESC	embryonic stem cell:	embryo
3	chr9:11618691-11618741	HCT-116	colon:	n/a
4	chr9:11618691-11618741	NHDF-neo	bronchial:	n/a
5	chr9:11618691-11618741	RPTEC	kidney:	n/a
6	chr9:11618265-11618315	NT2-D1	testis:	n/a
7	chr9:11618691-11618741	GM12892	blood:	n/a
8	chr9:11618265-11618315	HRE	kidney:	n/a
9	chr9:11618283-11618333	LNCaP	prostate:	n/a
10	chr9:11618691-11618741	Caco-2	colon:	n/a
11	chr9:11618283-11618333	HRE	kidney:	n/a
12	chr9:11618691-11618741	GM12891	blood:	n/a
13	chr9:11618691-11618741	HepG2	liver:	n/a
14	chr9:11618691-11618741	HEEpiC	esophagus:	n/a
15	chr9:11618265-11618315	PrEC	prostate:	n/a
16	chr9:11618691-11618741	SKMC	muscle:	n/a
17	chr9:11618265-11618315	BJ	skin:	n/a
18	chr9:11618265-11618315	NHDF-neo	bronchial:	n/a
19	chr9:11618265-11618315	A549	lung:	n/a
20	chr9:11618283-11618333	GM12891	blood:	n/a
21	chr9:11618691-11618741	U87	brain:	n/a
22	chr9:11618691-11618741	HRE	kidney:	n/a
23	chr9:11618283-11618333	ovcar-3	ovarian:	n/a
24	chr9:11618283-11618333	SK-N-MC	brain:	n/a
25	chr9:11618691-11618741	AG09309	skin:	n/a
26	chr9:11618691-11618741	BE2_C	brain:	n/a
27	chr9:11618265-11618315	SK-N-SH	brain:	n/a
28	chr9:11618691-11618741	H1-hESC	embryonic stem cell:	embryo
29	chr9:11618265-11618315	AoSMC	blood vessel:	n/a
30	chr9:11618265-11618315	HUVEC	blood vessel:	n/a
31	chr9:11618265-11618315	NHBE	bronchial:	n/a
32	chr9:11618283-11618333	AG04449	skin:	fetal
33	chr9:11618265-11618315	RPTEC	kidney:	n/a
34	chr9:11618265-11618315	Caco-2	colon:	n/a
35	chr9:11618283-11618333	SAEC	small airway:	n/a
36	chr9:11618691-11618741	HUVEC	blood vessel:	n/a
37	chr9:11618283-11618333	Hela-S3	cervix:	n/a
38	chr9:11618691-11618741	NT2-D1	testis:	n/a
39	chr9:11618265-11618315	HMEC	breast:	n/a
40	chr9:11618691-11618741	NHBE	bronchial:	n/a
41	chr9:11618283-11618333	NHDF-neo	bronchial:	n/a
42	chr9:11618691-11618741	BJ	skin:	n/a
43	chr9:11618265-11618315	IMR90	lung:	fetal
44	chr9:11618265-11618315	GM12891	blood:	n/a
45	chr9:11618283-11618333	Caco-2	colon:	n/a
46	chr9:11618265-11618315	AG04449	skin:	fetal
47	chr9:11618283-11618333	PFSK-1	brain:	n/a
48	chr9:11618283-11618333	HUVEC	blood vessel:	n/a
49	chr9:11618283-11618333	HRPEpiC	eye:	n/a
50	chr9:11618691-11618741	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10855589..10857004-chr9:11319142..11320476,6	MCF-7	breast:
2	chr9:11701463..11703909-chr9:11703963..11706145,2	K562	blood:
3	chr9:11701463..11703909-chr9:11703963..11706145,2	K562	blood:
4	chr11:62609117..62610638-chr9:11453391..11454911,2	K562	blood:
5	chr9:10855837..10856356-chr9:11319207..11319905,2	MCF-7	breast:
6	chr9:10366359..10367238-chr9:11319480..11320059,2	MCF-7	breast:
7	chr9:11653547..11655405-chr9:11656471..11658764,2	K562	blood:
8	chr9:11687941..11690802-chr9:11691495..11694345,3	K562	blood:
9	chr9:11687941..11690802-chr9:11691495..11694345,3	K562	blood:
10	chr9:11653547..11655405-chr9:11656471..11658764,2	K562	blood:
11	chr11:13082457..13083259-chr9:11319197..11319700,2	MCF-7	breast:
12	chr17:41381793..41383489-chr9:11453391..11454891,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-5	chr9:11829210-11829360	XLOC_007647
2	lnc-PTPRD-5	chr9:11829221-11829360	XLOC_007647
3	lnc-PTPRD-5	chr9:11822678-11822704	XLOC_007647
4	lnc-PTPRD-5	chr9:11834674-11834959	XLOC_007647
5	lnc-TYRP1-2	chr9:11277589-11277655	XLOC_007281
6	lnc-PTPRD-5	chr9:11826175-11826601	XLOC_007647
7	lnc-PTPRD-5	chr9:11829221-11829360	XLOC_007647
8	lnc-PTPRD-4	chr9:11276253-11276314	XLOC_007646
9	lnc-TYRP1-1	chr9:11313363-11313595	XLOC_007282
10	lnc-PTPRD-4	chr9:11275314-11275536	XLOC_007646
11	lnc-PTPRD-10	chr9:11824674-11824988	l_3733_chr9:11816028-11824988_testes
12	lnc-TYRP1-1	chr9:11325743-11325750	XLOC_007282
13	lnc-PTPRD-9	chr9:11265314-11265536	NONHSAT130211
14	lnc-PTPRD-10	chr9:11819221-11819360	l_3733_chr9:11816028-11824988_testes
15	lnc-PTPRD-10	chr9:11816029-11816601	l_3733_chr9:11816028-11824988_testes
16	lnc-PTPRD-9	chr9:11266253-11266314	NONHSAT130211
17	lnc-PTPRD-5	chr9:11834674-11834988	XLOC_007647
18	lnc-PTPRD-5	chr9:11834674-11834959	XLOC_007647
19	lnc-TYRP1-2	chr9:11277792-11277964	XLOC_007281

Variant related genes	Relation type
ENSG00000230365	TF binding region
ENSG00000230365	CpG island
ENSG00000236383	chromatin interactions
ENSG00000133316	chromatin interactions
CUL5	miRNA target sites
CSF1	miRNA target sites
FLOT2	miRNA target sites

Extended variants
information (count: 9738 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:9738 , 50 per page) page: 1 2 3 4 5 6 7 ... 195

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145556011	chr9:11233818-11233819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371904951	chr9:11233825-11233826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112908761	chr9:11233828-11233829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116938965	chr9:11233895-11233896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540494097	chr9:11233929-11233930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559735367	chr9:11233936-11233937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531943032	chr9:11233940-11233941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189999728	chr9:11233956-11233957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568659064	chr9:11233964-11233965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73405188	chr9:11233967-11233968	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs548535441	chr9:11233986-11233987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73405191	chr9:11234009-11234010	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs534245823	chr9:11234023-11234024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554471125	chr9:11234027-11234028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570865157	chr9:11234031-11234032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539794748	chr9:11234043-11234044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150429919	chr9:11234048-11234049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138193343	chr9:11234074-11234075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542289826	chr9:11234080-11234081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149565946	chr9:11234093-11234094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35085142	chr9:11234121-11234122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35557711	chr9:11234188-11234189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147254137	chr9:11234199-11234200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28691196	chr9:11234284-11234285	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs181590763	chr9:11234297-11234298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368179224	chr9:11234298-11234299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372547169	chr9:11234301-11234302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140689164	chr9:11234313-11234314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186005648	chr9:11234320-11234321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10125597	chr9:11234323-11234324	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190415671	chr9:11234348-11234349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573772066	chr9:11234349-11234350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562159162	chr9:11234396-11234397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534551961	chr9:11234398-11234399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527846013	chr9:11234434-11234435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548108963	chr9:11234435-11234436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571206030	chr9:11234441-11234442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184082932	chr9:11234452-11234453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550232309	chr9:11234456-11234457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570007539	chr9:11234510-11234511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73405194	chr9:11234521-11234522	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs553012523	chr9:11234525-11234526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555792423	chr9:11234526-11234527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536339431	chr9:11234527-11234528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574553312	chr9:11234591-11234592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148561541	chr9:11234592-11234593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553542218	chr9:11234611-11234612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10125665	chr9:11234615-11234616	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs545672330	chr9:11234619-11234620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7034246	chr9:11234635-11234636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	18511947	CNVD
Renal cell carcinoma	21215367	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chordoma	21215367	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11233800-11235200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:11234600-11235800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr9:11254200-11254800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr9:11257400-11258600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr9:11257600-11258000	Enhancers	Fetal Heart	heart
6	chr9:11258000-11258400	Flanking Active TSS	Fetal Heart	heart
7	chr9:11258200-11258600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr9:11258200-11258800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr9:11258200-11258800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr9:11258400-11259000	Enhancers	Fetal Heart	heart
11	chr9:11258800-11259800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr9:11259200-11260200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr9:11259400-11259800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:11259800-11260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:11268800-11269600	ZNF genes & repeats	Adipose Nuclei	Adipose
16	chr9:11280400-11281000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr9:11280600-11281000	Enhancers	Fetal Brain Female	brain
18	chr9:11280800-11281200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:11295400-11297000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:11296400-11296600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:11296600-11300800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:11297000-11297400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:11300800-11301000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:11312800-11313600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr9:11312800-11313600	Enhancers	Brain Hippocampus Middle	brain
26	chr9:11313000-11313400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:11313000-11313400	Enhancers	Brain Cingulate Gyrus	brain
28	chr9:11313000-11313600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr9:11313000-11313600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr9:11313000-11313800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr9:11313600-11314600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:11318000-11321800	Enhancers	Fetal Brain Male	brain
33	chr9:11318200-11319200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr9:11318200-11319800	Enhancers	Fetal Brain Female	brain
35	chr9:11318800-11320000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr9:11318800-11320200	Enhancers	Brain Germinal Matrix	brain
37	chr9:11319200-11320200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr9:11319600-11320400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:11319600-11320400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr9:11319800-11320800	Weak transcription	Fetal Brain Female	brain
41	chr9:11320800-11321600	Enhancers	Fetal Brain Female	brain
42	chr9:11321800-11322600	Weak transcription	Fetal Brain Male	brain
43	chr9:11322600-11322800	Enhancers	Fetal Brain Male	brain
44	chr9:11326000-11326400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr9:11328400-11328600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:11330400-11330600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:11330600-11330800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:11335000-11335600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:11337800-11338400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:11337800-11338600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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