Variant report

Variant	nsv892606
Chromosome Location	chr9:14588049-14697022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1193)
CpG islands
(count:549)
Chromatin interactive
region (count:37)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14661451-14661789	K562	blood:	n/a	n/a
2	ARID3A	chr9:14616384-14616695	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14616366-14616729	K562	blood:	n/a	n/a
4	ARID3A	chr9:14652772-14653234	HepG2	liver:	n/a	n/a
5	ATF1	chr9:14661502-14661775	K562	blood:	n/a	n/a
6	ATF2	chr9:14693237-14693620	GM12878	blood:	n/a	n/a
7	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
8	BACH1	chr9:14693258-14693548	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr9:14693199-14693708	GM12878	blood:	n/a	n/a
10	BCLAF1	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
11	BCLAF1	chr9:14693175-14693606	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:14692950-14693814	GM12878	blood:	n/a	chr9:14693117-14693133
14	BHLHE40	chr9:14616435-14616720	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
16	BRCA1	chr9:14652862-14653081	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr9:14654909-14655424	HCT-116	colon:	n/a	n/a
18	CBX3	chr9:14654902-14655428	HCT-116	colon:	n/a	n/a
19	CBX3	chr9:14654942-14655330	K562	blood:	n/a	n/a
20	CBX3	chr9:14593377-14593719	K562	blood:	n/a	n/a
21	CBX3	chr9:14654938-14655346	K562	blood:	n/a	n/a
22	CCNT2	chr9:14693300-14693572	K562	blood:	n/a	n/a
23	CEBPB	chr9:14593561-14593669	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:14687100-14687489	IMR90	lung:	n/a	n/a
25	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
26	CEBPB	chr9:14593410-14593662	K562	blood:	n/a	n/a
27	CEBPB	chr9:14640433-14640716	A549	lung:	n/a	n/a
28	CEBPB	chr9:14661506-14661801	K562	blood:	n/a	n/a
29	CEBPB	chr9:14620535-14620536	HepG2	liver:	n/a	n/a
30	CHD1	chr9:14693269-14693945	GM12878	blood:	n/a	n/a
31	CHD1	chr9:14688156-14688623	GM12878	blood:	n/a	n/a
32	CHD1	chr9:14693268-14693369	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr9:14693310-14693896	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr9:14616421-14616609	GM12878	blood:	n/a	n/a
35	CHD2	chr9:14692666-14692698	HepG2	liver:	n/a	n/a
36	CHD2	chr9:14692865-14693793	GM12878	blood:	n/a	chr9:14693027-14693037
37	CREB1	chr9:14693141-14693720	HepG2	liver:	n/a	n/a
38	CREB1	chr9:14693169-14693584	A549	lung:	n/a	n/a
39	CREB1	chr9:14652817-14653056	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr9:14693233-14693890	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr9:14616480-14616630	AG09309	skin:	n/a	n/a
42	CTCF	chr9:14616800-14616950	HVMF	connective:	n/a	n/a
43	CTCF	chr9:14661615-14661773	GM10248	blood:	n/a	chr9:14661642-14661663
44	CTCF	chr9:14652860-14653010	HMEC	breast:	n/a	n/a
45	CTCF	chr9:14661564-14661785	Spleen_OC	spleen:	n/a	chr9:14661642-14661663
46	CTCF	chr9:14661520-14661670	HCM	heart:	n/a	chr9:14661642-14661663
47	CTCF	chr9:14647990-14648127	K562	blood:	n/a	n/a
48	CTCF	chr9:14652840-14652990	Caco-2	colon:	n/a	n/a
49	CTCF	chr9:14653480-14653630	AG04450	lung:	n/a	n/a
50	CTCF	chr9:14652840-14652990	RPTEC	kidney:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14693082-14693132	ovcar-3	ovarian:	n/a
2	chr9:14692931-14692981	CMK	blood:	n/a
3	chr9:14691289-14691339	Jurkat	blood:	n/a
4	chr9:14691289-14691339	HRE	kidney:	n/a
5	chr9:14692931-14692981	NB4	blood:	n/a
6	chr9:14690531-14690581	GM19239	blood:	n/a
7	chr9:14643897-14643947	AG09309	skin:	n/a
8	chr9:14693648-14693698	PANC-1	pancreas:	n/a
9	chr9:14691289-14691339	GM06990	blood:	n/a
10	chr9:14693538-14693588	CMK	blood:	n/a
11	chr9:14691289-14691339	PFSK-1	brain:	n/a
12	chr9:14693888-14693938	MCF-7	breast:	n/a
13	chr9:14693082-14693132	IMR90	lung:	fetal
14	chr9:14643897-14643947	MCF-7	breast:	n/a
15	chr9:14693888-14693938	GM19239	blood:	n/a
16	chr9:14690531-14690581	SK-N-MC	brain:	n/a
17	chr9:14693504-14693554	HCPEpiC	choroid plexus:	n/a
18	chr9:14693888-14693938	GM06990	blood:	n/a
19	chr9:14693504-14693554	Jurkat	blood:	n/a
20	chr9:14693648-14693698	AG04449	skin:	fetal
21	chr9:14693538-14693588	PrEC	prostate:	n/a
22	chr9:14692931-14692981	Jurkat	blood:	n/a
23	chr9:14693082-14693132	K562	blood:	n/a
24	chr9:14693082-14693132	HRE	kidney:	n/a
25	chr9:14693888-14693938	SK-N-SH	brain:	n/a
26	chr9:14693082-14693132	HCPEpiC	choroid plexus:	n/a
27	chr9:14691289-14691339	HUVEC	blood vessel:	n/a
28	chr9:14690531-14690581	GM12891	blood:	n/a
29	chr9:14693538-14693588	BJ	skin:	n/a
30	chr9:14690531-14690581	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:14693888-14693938	SK-N-SH_RA	brain:	n/a
32	chr9:14693538-14693588	HRE	kidney:	n/a
33	chr9:14692931-14692981	HMEC	breast:	n/a
34	chr9:14693082-14693132	PANC-1	pancreas:	n/a
35	chr9:14643897-14643947	GM12892	blood:	n/a
36	chr9:14693888-14693938	AG09319	gingival:	n/a
37	chr9:14693082-14693132	Caco-2	colon:	n/a
38	chr9:14692931-14692981	HNPCEpiC	eye:	n/a
39	chr9:14693082-14693132	AG09319	gingival:	n/a
40	chr9:14693648-14693698	HAEpiC	amniotic membrane:	n/a
41	chr9:14693888-14693938	SAEC	small airway:	n/a
42	chr9:14693648-14693698	Hepatocyte	liver:	n/a
43	chr9:14692931-14692981	HEK293	kidney:	embryo
44	chr9:14693504-14693554	NHDF-neo	bronchial:	n/a
45	chr9:14643897-14643947	PrEC	prostate:	n/a
46	chr9:14693648-14693698	NB4	blood:	n/a
47	chr9:14643897-14643947	HEK293	kidney:	embryo
48	chr9:14643897-14643947	SAEC	small airway:	n/a
49	chr9:14693504-14693554	H1-hESC	embryonic stem cell:	embryo
50	chr9:14693888-14693938	HRPEpiC	eye:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
2	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
3	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
4	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
5	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
6	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
7	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
8	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
9	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
10	chr9:14442256..14442845-chr9:14661275..14662107,4	K562	blood:
11	chr9:14676498..14678344-chr9:14692478..14694843,2	MCF-7	breast:
12	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
13	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
14	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
15	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
16	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
17	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
18	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
19	chr9:14607657..14609554-chr9:14615392..14617575,2	K562	blood:
20	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:
21	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
22	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
23	chr9:14607927..14609572-chr9:14611159..14613571,2	MCF-7	breast:
24	chr9:14464938..14465658-chr9:14661578..14662250,2	MCF-7	breast:
25	chr9:14627684..14629345-chr9:14693335..14694855,2	MCF-7	breast:
26	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
27	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
28	chr9:14465253..14465899-chr9:14652688..14653342,2	MCF-7	breast:
29	chr9:14594819..14596399-chr9:14599180..14601861,2	K562	blood:
30	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
31	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
32	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
33	chr9:14465217..14466121-chr9:14652305..14653436,3	K562	blood:
34	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
35	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
36	chr9:14442114..14442886-chr9:14652552..14653366,4	MCF-7	breast:
37	chr9:14594419..14596910-chr9:14651251..14653446,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC21-2	chr9:14606167-14606546	NONHSAT130251
2	lnc-C9orf146-8	chr9:14593575-14594198	NONHSAT130250
3	lnc-C9orf146-7	chr9:14588065-14588629	NONHSAT130249
4	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254
5	lnc-ZDHHC21-3	chr9:14588795-14590063	ENSG00000272871.1
6	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
7	lnc-CER1-1	chr9:14693227-14693263	NONHSAT130254
8	lnc-ZDHHC21-1	chr9:14611070-14614754	NONHSAT130252
9	lnc-C9orf146-7	chr9:14588795-14589277	NONHSAT130249
10	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
11	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254
12	lnc-ZDHHC21-2	chr9:14609848-14609996	NONHSAT130251

No data

Variant related genes	Relation type
ZDHHC21	TF binding region
ENSG00000272871	TF binding region
ENSG00000273399	TF binding region
ENSG00000229029	TF binding region
ZDHHC21	CpG island
ENSG00000272871	CpG island
ENSG00000273399	CpG island
ENSG00000229029	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 5255 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5255 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12238310	chr9:14588049-14588050	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34980241	chr9:14588053-14588054	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs10961600	chr9:14588059-14588060	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs542029973	chr9:14588106-14588107	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs561676165	chr9:14588133-14588134	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs150131822	chr9:14588140-14588141	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs540675379	chr9:14588201-14588202	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs564071292	chr9:14588231-14588232	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs138694843	chr9:14588245-14588246	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs564548767	chr9:14588249-14588250	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs562818702	chr9:14588254-14588255	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs540343509	chr9:14588268-14588269	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs531819379	chr9:14588271-14588272	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs548754134	chr9:14588279-14588280	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs568507851	chr9:14588339-14588340	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs146284738	chr9:14588340-14588341	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs547482341	chr9:14588361-14588362	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs533421295	chr9:14588372-14588373	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs368588839	chr9:14588386-14588387	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs187153116	chr9:14588404-14588405	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs556532668	chr9:14588416-14588417	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs62532699	chr9:14588433-14588434	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs576395272	chr9:14588436-14588437	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs535339874	chr9:14588439-14588440	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs371106240	chr9:14588466-14588467	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs555495049	chr9:14588471-14588472	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs572058628	chr9:14588474-14588475	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs150655790	chr9:14588479-14588480	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs61323969	chr9:14588480-14588481	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs558347543	chr9:14588486-14588487	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs12337282	chr9:14588497-14588498	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs35305265	chr9:14588498-14588499	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs191253609	chr9:14588528-14588529	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs137881445	chr9:14588623-14588624	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs16932034	chr9:14588676-14588677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183801473	chr9:14588694-14588695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571642165	chr9:14588745-14588746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531879124	chr9:14588753-14588754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548498905	chr9:14588755-14588756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577495710	chr9:14588807-14588808	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs562267089	chr9:14588857-14588858	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs186678570	chr9:14588897-14588898	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs1047720	chr9:14588910-14588911	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs117840217	chr9:14588915-14588916	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs1047718	chr9:14588923-14588924	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550197967	chr9:14588932-14588933	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs193210622	chr9:14588936-14588937	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs185606510	chr9:14588951-14588952	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs376140377	chr9:14588958-14588959	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs116792264	chr9:14588970-14588971	Weak transcription	lncRNA	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:1672 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14577400-14597200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:14577600-14596200	Weak transcription	Pancreas	Pancrea
3	chr9:14582400-14596200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:14585200-14589000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:14585800-14598000	Weak transcription	Right Ventricle	heart
6	chr9:14586000-14592000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr9:14586000-14596200	Weak transcription	Lung	lung
8	chr9:14586000-14597000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr9:14586200-14595200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr9:14586400-14595800	Weak transcription	Brain Germinal Matrix	brain
11	chr9:14586600-14595200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr9:14586800-14593400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr9:14586800-14629800	Weak transcription	Primary T cells from cord blood	blood
14	chr9:14587200-14591600	Weak transcription	GM12878-XiMat	blood
15	chr9:14587400-14595800	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr9:14587600-14595600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr9:14587600-14596200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr9:14587600-14596200	Weak transcription	Left Ventricle	heart
19	chr9:14587600-14599600	Weak transcription	Placenta	Placenta
20	chr9:14587800-14588200	Strong transcription	Aorta	Aorta
21	chr9:14587800-14618400	Weak transcription	HUVEC	blood vessel
22	chr9:14588000-14596000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr9:14588200-14589000	Weak transcription	Aorta	Aorta
24	chr9:14588200-14591200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:14588200-14618800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr9:14588800-14595800	Weak transcription	Liver	Liver
27	chr9:14588800-14595800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr9:14589000-14589400	Strong transcription	Aorta	Aorta
29	chr9:14589000-14589600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:14589000-14596000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr9:14589400-14593600	Weak transcription	Aorta	Aorta
32	chr9:14589600-14594400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:14591800-14593400	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr9:14592000-14596200	Weak transcription	Ovary	ovary
35	chr9:14592800-14595200	Weak transcription	Primary B cells from cord blood	blood
36	chr9:14593400-14593600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
37	chr9:14593400-14593800	Enhancers	HepG2	liver
38	chr9:14593400-14594000	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr9:14593400-14594000	ZNF genes & repeats	Gastric	stomach
40	chr9:14593400-14594000	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr9:14593400-14595400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr9:14593600-14593800	Weak transcription	Osteobl	bone
43	chr9:14593600-14594000	ZNF genes & repeats	Aorta	Aorta
44	chr9:14593600-14594000	ZNF genes & repeats	Esophagus	oesophagus
45	chr9:14593800-14594000	ZNF genes & repeats	Osteobl	bone
46	chr9:14593800-14594200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:14594000-14595400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr9:14594000-14596200	Weak transcription	Aorta	Aorta
49	chr9:14594000-14596200	Weak transcription	Esophagus	oesophagus
50	chr9:14594000-14596200	Weak transcription	Gastric	stomach

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