Variant report

Variant	esv2752921
Chromosome Location	chr9:14593749-14694372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1164)
CpG islands
(count:552)
Chromatin interactive
region (count:37)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1164 , 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	chr9:14616366-14616729	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	chr9:14693237-14693620	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	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
10	BCLAF1	chr9:14693199-14693708	GM12878	blood:	n/a	n/a
11	BCLAF1	chr9:14693175-14693606	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:14692950-14693814	GM12878	blood:	n/a	chr9:14693117-14693133
13	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:14616435-14616720	GM12878	blood:	n/a	n/a
16	BRCA1	chr9:14652862-14653081	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr9:14654942-14655330	K562	blood:	n/a	n/a
18	CBX3	chr9:14654902-14655428	HCT-116	colon:	n/a	n/a
19	CBX3	chr9:14654938-14655346	K562	blood:	n/a	n/a
20	CBX3	chr9:14654909-14655424	HCT-116	colon:	n/a	n/a
21	CCNT2	chr9:14693300-14693572	K562	blood:	n/a	n/a
22	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
23	CEBPB	chr9:14661506-14661801	K562	blood:	n/a	n/a
24	CEBPB	chr9:14687100-14687489	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:14620535-14620536	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:14640433-14640716	A549	lung:	n/a	n/a
27	CHD1	chr9:14693269-14693945	GM12878	blood:	n/a	n/a
28	CHD1	chr9:14688156-14688623	GM12878	blood:	n/a	n/a
29	CHD1	chr9:14693268-14693369	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr9:14693310-14693896	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:14692666-14692698	HepG2	liver:	n/a	n/a
32	CHD2	chr9:14616421-14616609	GM12878	blood:	n/a	n/a
33	CHD2	chr9:14692865-14693793	GM12878	blood:	n/a	chr9:14693027-14693037
34	CREB1	chr9:14652817-14653056	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr9:14693169-14693584	A549	lung:	n/a	n/a
36	CREB1	chr9:14693141-14693720	HepG2	liver:	n/a	n/a
37	CTBP2	chr9:14693233-14693890	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:14616560-14616710	HCM	heart:	n/a	n/a
39	CTCF	chr9:14616520-14616670	Caco-2	colon:	n/a	n/a
40	CTCF	chr9:14616460-14616610	GM12871	blood:	n/a	n/a
41	CTCF	chr9:14693260-14693410	AG04449	skin:	n/a	n/a
42	CTCF	chr9:14652806-14653083	HepG2	liver:	n/a	n/a
43	CTCF	chr9:14692935-14693471	GM12878	blood:	n/a	n/a
44	CTCF	chr9:14661540-14661690	GM12872	blood:	n/a	chr9:14661642-14661663
45	CTCF	chr9:14652840-14652990	RPTEC	kidney:	n/a	n/a
46	CTCF	chr9:14652980-14653130	A549	lung:	n/a	n/a
47	CTCF	chr9:14598797-14598872	Fibrobl	skin:	n/a	n/a
48	CTCF	chr9:14616454-14616677	LNCaP	prostate:	n/a	n/a
49	CTCF	chr9:14652940-14653090	AG09309	skin:	n/a	n/a
50	CTCF	chr9:14652860-14653010	AG04450	lung:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14692931-14692981	GM19239	blood:	n/a
2	chr9:14693082-14693132	SK-N-SH_RA	brain:	n/a
3	chr9:14691289-14691339	HRE	kidney:	n/a
4	chr9:14692931-14692981	GM19239	blood:	n/a
5	chr9:14693082-14693132	SK-N-SH_RA	brain:	n/a
6	chr9:14691289-14691339	HRE	kidney:	n/a
7	chr9:14643897-14643947	AG10803	skin:	n/a
8	chr9:14693888-14693938	ovcar-3	ovarian:	n/a
9	chr9:14693082-14693132	HAEpiC	amniotic membrane:	n/a
10	chr9:14693538-14693588	HRE	kidney:	n/a
11	chr9:14693888-14693938	AG04450	lung:	fetal
12	chr9:14693082-14693132	HEK293	kidney:	embryo
13	chr9:14693504-14693554	A549	lung:	n/a
14	chr9:14693648-14693698	IMR90	lung:	fetal
15	chr9:14693648-14693698	T-47D	breast:	n/a
16	chr9:14693538-14693588	BE2_C	brain:	n/a
17	chr9:14693082-14693132	NH-A	brain:	n/a
18	chr9:14643897-14643947	GM12892	blood:	n/a
19	chr9:14693888-14693938	HPAEpiC	pulmonary alveolar:	n/a
20	chr9:14692931-14692981	ProgFib	skin:	n/a
21	chr9:14693648-14693698	NHBE	bronchial:	n/a
22	chr9:14693888-14693938	HUVEC	blood vessel:	n/a
23	chr9:14691289-14691339	NH-A	brain:	n/a
24	chr9:14643897-14643947	HRPEpiC	eye:	n/a
25	chr9:14691289-14691339	SAEC	small airway:	n/a
26	chr9:14693082-14693132	HCF	heart:	n/a
27	chr9:14693648-14693698	PANC-1	pancreas:	n/a
28	chr9:14693082-14693132	HRPEpiC	eye:	n/a
29	chr9:14693888-14693938	PrEC	prostate:	n/a
30	chr9:14693538-14693588	MCF10A-Er-Src	breast:	n/a
31	chr9:14692931-14692981	NT2-D1	testis:	n/a
32	chr9:14693082-14693132	HL-60	blood:	n/a
33	chr9:14693538-14693588	HRPEpiC	eye:	n/a
34	chr9:14691289-14691339	MCF10A-Er-Src	breast:	n/a
35	chr9:14691289-14691339	K562	blood:	n/a
36	chr9:14693504-14693554	SKMC	muscle:	n/a
37	chr9:14643897-14643947	HAEpiC	amniotic membrane:	n/a
38	chr9:14691289-14691339	BE2_C	brain:	n/a
39	chr9:14693504-14693554	HIPEpiC	eye:	n/a
40	chr9:14693082-14693132	RPTEC	kidney:	n/a
41	chr9:14693888-14693938	BE2_C	brain:	n/a
42	chr9:14693888-14693938	HCPEpiC	choroid plexus:	n/a
43	chr9:14691289-14691339	ProgFib	skin:	n/a
44	chr9:14692931-14692981	A549	lung:	n/a
45	chr9:14691289-14691339	Jurkat	blood:	n/a
46	chr9:14643897-14643947	HRCEpiC	kidney:	n/a
47	chr9:14693888-14693938	Hela-S3	cervix:	n/a
48	chr9:14692931-14692981	CMK	blood:	n/a
49	chr9:14693648-14693698	Caco-2	colon:	n/a
50	chr9:14643897-14643947	HL-60	blood:	n/a

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

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

(count:9 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 4874 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:4874 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1410303	chr9:14593749-14593750	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543708746	chr9:14593769-14593770	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs1410302	chr9:14593774-14593775	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs543082968	chr9:14593859-14593860	Weak transcription ZNF genes & repeats Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs150079723	chr9:14593900-14593901	Weak transcription ZNF genes & repeats Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs561484034	chr9:14593920-14593921	Weak transcription ZNF genes & repeats Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs554141966	chr9:14593934-14593935	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs181895980	chr9:14593935-14593936	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs72605692	chr9:14593977-14593978	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556353426	chr9:14594004-14594005	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs185718381	chr9:14594029-14594030	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs541882132	chr9:14594040-14594041	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs112095061	chr9:14594048-14594049	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs138397600	chr9:14594063-14594064	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs572043846	chr9:14594071-14594072	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs540617921	chr9:14594082-14594083	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs190548994	chr9:14594094-14594095	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs532617887	chr9:14594109-14594110	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs116256251	chr9:14594146-14594147	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs182426092	chr9:14594154-14594155	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs149266669	chr9:14594182-14594183	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs548690237	chr9:14594186-14594187	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs76049349	chr9:14594187-14594188	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs79069018	chr9:14594205-14594206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547808509	chr9:14594212-14594213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570769621	chr9:14594233-14594234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568603719	chr9:14594261-14594262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77814883	chr9:14594274-14594275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74566189	chr9:14594300-14594301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77249422	chr9:14594301-14594302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59569307	chr9:14594328-14594329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10756583	chr9:14594350-14594351	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs569861572	chr9:14594352-14594353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535279528	chr9:14594356-14594357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555481030	chr9:14594357-14594358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533211945	chr9:14594370-14594371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537980778	chr9:14594394-14594395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12003843	chr9:14594407-14594408	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557287584	chr9:14594414-14594415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201214720	chr9:14594456-14594457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200099025	chr9:14594457-14594458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559400371	chr9:14594461-14594462	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs11794863	chr9:14594501-14594502	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs546057852	chr9:14594507-14594508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371652176	chr9:14594516-14594517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78152156	chr9:14594529-14594530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140920460	chr9:14594538-14594539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544025181	chr9:14594539-14594540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143165186	chr9:14594571-14594572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10756584	chr9:14594594-14594595	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1657 , 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	chr9:14585800-14598000	Weak transcription	Right Ventricle	heart
5	chr9:14586000-14596200	Weak transcription	Lung	lung
6	chr9:14586000-14597000	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr9:14586200-14595200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr9:14586400-14595800	Weak transcription	Brain Germinal Matrix	brain
9	chr9:14586600-14595200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:14586800-14629800	Weak transcription	Primary T cells from cord blood	blood
11	chr9:14587400-14595800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr9:14587600-14595600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:14587600-14596200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr9:14587600-14596200	Weak transcription	Left Ventricle	heart
15	chr9:14587600-14599600	Weak transcription	Placenta	Placenta
16	chr9:14587800-14618400	Weak transcription	HUVEC	blood vessel
17	chr9:14588000-14596000	Weak transcription	Brain Cingulate Gyrus	brain
18	chr9:14588200-14618800	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr9:14588800-14595800	Weak transcription	Liver	Liver
20	chr9:14588800-14595800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr9:14589000-14596000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr9:14589600-14594400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:14592000-14596200	Weak transcription	Ovary	ovary
24	chr9:14592800-14595200	Weak transcription	Primary B cells from cord blood	blood
25	chr9:14593400-14593800	Enhancers	HepG2	liver
26	chr9:14593400-14594000	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr9:14593400-14594000	ZNF genes & repeats	Gastric	stomach
28	chr9:14593400-14594000	Strong transcription	Skeletal Muscle Female	skeletal muscle
29	chr9:14593400-14595400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr9:14593600-14593800	Weak transcription	Osteobl	bone
31	chr9:14593600-14594000	ZNF genes & repeats	Aorta	Aorta
32	chr9:14593600-14594000	ZNF genes & repeats	Esophagus	oesophagus
33	chr9:14593800-14594000	ZNF genes & repeats	Osteobl	bone
34	chr9:14593800-14594200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:14594000-14595400	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr9:14594000-14596200	Weak transcription	Aorta	Aorta
37	chr9:14594000-14596200	Weak transcription	Esophagus	oesophagus
38	chr9:14594000-14596200	Weak transcription	Gastric	stomach
39	chr9:14594000-14596400	Weak transcription	Fetal Intestine Small	intestine
40	chr9:14594000-14599800	Weak transcription	Osteobl	bone
41	chr9:14594200-14608800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr9:14594400-14596200	Weak transcription	Fetal Stomach	stomach
43	chr9:14594400-14596600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:14594400-14618200	Weak transcription	NH-A	brain
45	chr9:14594600-14595200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:14594600-14596200	Weak transcription	Fetal Intestine Large	intestine
47	chr9:14594800-14633400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr9:14595000-14595800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr9:14595000-14596000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr9:14595000-14596400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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