Variant report

Variant	nsv427838
Chromosome Location	chr9:13229753-13393890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1089)
CpG islands
(count:671)
Chromatin interactive
region (count:35)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:13267952-13268141	K562	blood:	n/a	n/a
2	ARID3A	chr9:13269505-13269999	K562	blood:	n/a	n/a
3	ARID3A	chr9:13268423-13268869	K562	blood:	n/a	n/a
4	ATF1	chr9:13268465-13268833	K562	blood:	n/a	n/a
5	ATF1	chr9:13278032-13278621	K562	blood:	n/a	n/a
6	ATF1	chr9:13267768-13268030	K562	blood:	n/a	n/a
7	ATF3	chr9:13268444-13268740	K562	blood:	n/a	n/a
8	BACH1	chr9:13279363-13279954	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:13367921-13368142	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:13278144-13278639	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr9:13278045-13278680	K562	blood:	n/a	n/a
12	BHLHE40	chr9:13315456-13315474	K562	blood:	n/a	n/a
13	BHLHE40	chr9:13279384-13279648	K562	blood:	n/a	n/a
14	CBX3	chr9:13268543-13268820	K562	blood:	n/a	n/a
15	CCNT2	chr9:13278210-13278873	K562	blood:	n/a	n/a
16	CCNT2	chr9:13279271-13279892	K562	blood:	n/a	chr9:13279622-13279631
17	CEBPB	chr9:13274909-13275601	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:13267750-13268132	IMR90	lung:	n/a	chr9:13268032-13268045
19	CEBPB	chr9:13261370-13261575	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:13235169-13235395	A549	lung:	n/a	n/a
21	CEBPD	chr9:13268451-13268876	K562	blood:	n/a	n/a
22	CEBPD	chr9:13279233-13279576	HepG2	liver:	n/a	n/a
23	CHD2	chr9:13278431-13278782	H1-hESC	embryonic stem cell:	n/a	chr9:13278434-13278444
24	CHD2	chr9:13279455-13279700	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr9:13279452-13279788	K562	blood:	n/a	n/a
26	CHD2	chr9:13279406-13279700	HepG2	liver:	n/a	n/a
27	CHD2	chr9:13279436-13279848	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr9:13278750-13278753	HepG2	liver:	n/a	n/a
29	CREB1	chr9:13277932-13278478	K562	blood:	n/a	chr9:13278215-13278228
30	CREB1	chr9:13279395-13279883	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr9:13279252-13279948	HepG2	liver:	n/a	n/a
32	CREB1	chr9:13279298-13279841	A549	lung:	n/a	n/a
33	CREB1	chr9:13278371-13278850	A549	lung:	n/a	n/a
34	CTBP2	chr9:13278130-13279032	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr9:13384340-13384490	SAEC	small airway:	n/a	n/a
36	CTCF	chr9:13363541-13363625	LNCaP	prostate:	n/a	n/a
37	CTCF	chr9:13291740-13291890	HCFaa	heart:	n/a	n/a
38	CTCF	chr9:13351880-13352030	GM12873	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
39	CTCF	chr9:13278800-13278950	HPAF	blood vessel:	n/a	chr9:13278914-13278927 chr9:13278884-13278897
40	CTCF	chr9:13351960-13352110	GM12865	blood:	n/a	n/a
41	CTCF	chr9:13351920-13352070	GM12867	blood:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
42	CTCF	chr9:13278829-13278832	K562	blood:	n/a	n/a
43	CTCF	chr9:13278860-13279010	HFF	foreskin:	n/a	chr9:13278914-13278927 chr9:13278884-13278897
44	CTCF	chr9:13351880-13352030	NHDF-neo	bronchial:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
45	CTCF	chr9:13291720-13291870	AG04450	lung:	n/a	n/a
46	CTCF	chr9:13291860-13292010	BE2_C	brain:	n/a	n/a
47	CTCF	chr9:13351840-13351990	HCT-116	colon:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
48	CTCF	chr9:13351820-13351970	NHEK	skin:	n/a	n/a
49	CTCF	chr9:13351860-13352010	HCT-116	colon:	n/a	chr9:13351959-13351980 chr9:13351958-13351974 chr9:13351957-13351975
50	CTCF	chr9:13351420-13351570	SAEC	small airway:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13323130-13323180	HRCEpiC	kidney:	n/a
2	chr9:13249504-13249554	ProgFib	skin:	n/a
3	chr9:13251228-13251278	HIPEpiC	eye:	n/a
4	chr9:13251228-13251278	HCT-116	colon:	n/a
5	chr9:13278977-13279027	GM06990	blood:	n/a
6	chr9:13284899-13284949	HL-60	blood:	n/a
7	chr9:13251228-13251278	GM06990	blood:	n/a
8	chr9:13278512-13278562	ovcar-3	ovarian:	n/a
9	chr9:13251431-13251481	SK-N-SH_RA	brain:	n/a
10	chr9:13251228-13251278	HUVEC	blood vessel:	n/a
11	chr9:13278626-13278676	AG10803	skin:	n/a
12	chr9:13249504-13249554	GM12892	blood:	n/a
13	chr9:13284899-13284949	NHDF-neo	bronchial:	n/a
14	chr9:13278512-13278562	GM19239	blood:	n/a
15	chr9:13284899-13284949	PrEC	prostate:	n/a
16	chr9:13323130-13323180	CMK	blood:	n/a
17	chr9:13278977-13279027	GM12891	blood:	n/a
18	chr9:13323130-13323180	HMEC	breast:	n/a
19	chr9:13279482-13279532	SKMC	muscle:	n/a
20	chr9:13251228-13251278	HEK293	kidney:	embryo
21	chr9:13323130-13323180	NHDF-neo	bronchial:	n/a
22	chr9:13251431-13251481	RPTEC	kidney:	n/a
23	chr9:13251431-13251481	NHDF-neo	bronchial:	n/a
24	chr9:13279482-13279532	HCM	heart:	n/a
25	chr9:13278512-13278562	Hepatocyte	liver:	n/a
26	chr9:13323130-13323180	GM12878	blood:	n/a
27	chr9:13249504-13249554	NHDF-neo	bronchial:	n/a
28	chr9:13249504-13249554	IMR90	lung:	fetal
29	chr9:13323130-13323180	ECC-1	luminal epithelium:	n/a
30	chr9:13278977-13279027	SK-N-SH_RA	brain:	n/a
31	chr9:13323130-13323180	A549	lung:	n/a
32	chr9:13251228-13251278	NHDF-neo	bronchial:	n/a
33	chr9:13279482-13279532	MCF10A-Er-Src	breast:	n/a
34	chr9:13323130-13323180	HCPEpiC	choroid plexus:	n/a
35	chr9:13251431-13251481	GM12878	blood:	n/a
36	chr9:13284899-13284949	SK-N-MC	brain:	n/a
37	chr9:13280025-13280075	Hepatocyte	liver:	n/a
38	chr9:13278977-13279027	PrEC	prostate:	n/a
39	chr9:13278977-13279027	ECC-1	luminal epithelium:	n/a
40	chr9:13279482-13279532	U87	brain:	n/a
41	chr9:13279482-13279532	SK-N-SH_RA	brain:	n/a
42	chr9:13251431-13251481	U87	brain:	n/a
43	chr9:13323130-13323180	MCF10A-Er-Src	breast:	n/a
44	chr9:13279482-13279532	HMEC	breast:	n/a
45	chr9:13278977-13279027	PFSK-1	brain:	n/a
46	chr9:13279482-13279532	HRE	kidney:	n/a
47	chr9:13280025-13280075	BJ	skin:	n/a
48	chr9:13279482-13279532	HUVEC	blood vessel:	n/a
49	chr9:13278626-13278676	SK-N-SH_RA	brain:	n/a
50	chr9:13284899-13284949	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:13230183..13232341-chr9:13234177..13235807,2	MCF-7	breast:
2	chr9:13281407..13283656-chr9:13286644..13288961,2	MCF-7	breast:
3	chr9:13256063..13258580-chr9:13259796..13261728,2	MCF-7	breast:
4	chr9:13266586..13268806-chr9:13275605..13278055,2	MCF-7	breast:
5	chr9:13033734..13035793-chr9:13280439..13283221,2	K562	blood:
6	chr9:13257934..13260781-chr9:13265128..13267553,2	K562	blood:
7	chr9:13257934..13260781-chr9:13265128..13267553,2	K562	blood:
8	chr9:13245657..13247575-chr9:13257459..13259209,2	MCF-7	breast:
9	chr9:13278089..13282078-chr9:14313109..14316114,3	MCF-7	breast:
10	chr9:13287399..13289604-chr9:13290158..13292995,2	K562	blood:
11	chr17:55977919..55980808-chr9:13278471..13279995,2	MCF-7	breast:
12	chr9:13277467..13280147-chr9:13286399..13289258,3	MCF-7	breast:
13	chr9:13261386..13263235-chr9:13277146..13279520,2	MCF-7	breast:
14	chr9:13351598..13352233-chr9:14353302..14354081,2	MCF-7	breast:
15	chr9:13256063..13258580-chr9:13259796..13261728,2	MCF-7	breast:
16	chr9:13267404..13273261-chr9:13274037..13279578,8	K562	blood:
17	chr9:13227295..13229314-chr9:13231919..13233666,2	K562	blood:
18	chr8:112133641..112134299-chr9:13359583..13360482,2	MCF-7	breast:
19	chr9:13245657..13247575-chr9:13257459..13259209,2	MCF-7	breast:
20	chr9:13370327..13372389-chr9:13372731..13374721,2	MCF-7	breast:
21	chr9:13236159..13239673-chr9:13240021..13241602,3	K562	blood:
22	chr9:13278476..13280409-chr9:13296744..13299210,3	MCF-7	breast:
23	chr9:13275549..13278427-chr9:13279998..13281670,2	K562	blood:
24	chr9:13236159..13239673-chr9:13240021..13241602,3	K562	blood:
25	chr9:13230183..13232341-chr9:13234177..13235807,2	MCF-7	breast:
26	chr9:13275549..13278427-chr9:13279998..13281670,2	K562	blood:
27	chr9:13370327..13372389-chr9:13372731..13374721,2	MCF-7	breast:
28	chr9:13276562..13283255-chr9:13284283..13286656,6	MCF-7	breast:
29	chr9:13278596..13280107-chr9:13281623..13284453,2	MCF-7	breast:
30	chr9:13266536..13270627-chr9:13277145..13281714,5	K562	blood:
31	chr9:13287399..13289604-chr9:13290158..13292995,2	K562	blood:
32	chr9:13266586..13268806-chr9:13275605..13278055,2	MCF-7	breast:
33	chr9:13281407..13283656-chr9:13286644..13288961,2	MCF-7	breast:
34	chr9:13253272..13256171-chr9:13277669..13280982,3	MCF-7	breast:
35	chr9:13351470..13352357-chr9:13423813..13424815,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-3	chr9:13322805-13323449	NONHSAT130234
2	lnc-NFIB-1	chr9:13276573-13276770	ENSG00000234740.1
3	lnc-NFIB-1	chr9:13274509-13274609	ENSG00000234740.1
4	lnc-NFIB-1	chr9:13279029-13279186	ENSG00000234740.1

No data

Variant related genes	Relation type
MPDZ	TF binding region
ENSG00000223672	TF binding region
ENSG00000234740	TF binding region
MPDZ	CpG island
ENSG00000223672	CpG island
ENSG00000234740	CpG island
ENSG00000234740	chromatin interactions
ENSG00000180891	chromatin interactions
ENSG00000147862	chromatin interactions
ENSG00000107186	chromatin interactions

Extended variants
information (count: 5285 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:5285 , 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	rs190757170	chr9:13229777-13229778	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538561586	chr9:13229851-13229852	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4145185	chr9:13229885-13229886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183191408	chr9:13230001-13230002	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139825004	chr9:13230024-13230025	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537692650	chr9:13230032-13230033	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554455541	chr9:13230092-13230093	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574086955	chr9:13230098-13230099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148151178	chr9:13230119-13230120	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542710092	chr9:13230184-13230185	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376893478	chr9:13230185-13230186	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115560494	chr9:13230186-13230187	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116758252	chr9:13230194-13230195	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545406862	chr9:13230218-13230219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565605895	chr9:13230219-13230220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531228795	chr9:13230227-13230228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141840342	chr9:13230229-13230230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79825924	chr9:13230234-13230235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529816994	chr9:13230241-13230242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72706378	chr9:13230265-13230266	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561219959	chr9:13230266-13230267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10809919	chr9:13230289-13230290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551749664	chr9:13230315-13230316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188898258	chr9:13230343-13230344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537705599	chr9:13230355-13230356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150634377	chr9:13230387-13230388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559124231	chr9:13230401-13230402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575793472	chr9:13230406-13230407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193153566	chr9:13230435-13230436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553228087	chr9:13230477-13230478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200176792	chr9:13230479-13230480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545466258	chr9:13230514-13230515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558984156	chr9:13230517-13230518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74882051	chr9:13230527-13230528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185336344	chr9:13230531-13230532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576018234	chr9:13230564-13230565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34964885	chr9:13230583-13230584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs80188599	chr9:13230642-13230643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561545199	chr9:13230650-13230651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530262739	chr9:13230654-13230655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188093933	chr9:13230655-13230656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540796443	chr9:13230690-13230691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78422911	chr9:13230705-13230706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377719393	chr9:13230730-13230731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532068822	chr9:13230765-13230766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116127970	chr9:13230793-13230794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554420444	chr9:13230807-13230808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533126282	chr9:13230857-13230858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568466962	chr9:13230907-13230908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369100908	chr9:13230931-13230932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
abnormal development	18461090	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	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
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13164200-13248600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:13164200-13258800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:13189000-13268600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:13190400-13237800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:13202800-13250600	Weak transcription	Pancreas	Pancrea
6	chr9:13202800-13250800	Weak transcription	Psoas Muscle	Psoas
7	chr9:13203000-13261000	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:13203400-13247000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr9:13203600-13245600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:13204000-13241800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:13204000-13249200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:13204200-13244600	Weak transcription	HepG2	liver
13	chr9:13206000-13247000	Weak transcription	Brain Angular Gyrus	brain
14	chr9:13208200-13265000	Weak transcription	Aorta	Aorta
15	chr9:13209800-13266000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr9:13215800-13233200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:13216600-13247000	Weak transcription	Fetal Brain Female	brain
18	chr9:13217000-13244200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr9:13218200-13231800	Weak transcription	NH-A	brain
20	chr9:13219600-13232800	Weak transcription	NHDF-Ad	bronchial
21	chr9:13219800-13265600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr9:13221600-13241600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr9:13221600-13244200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:13221600-13245400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:13221800-13242800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr9:13221800-13246600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:13222600-13238000	Weak transcription	Adipose Nuclei	Adipose
28	chr9:13222600-13246200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr9:13223800-13239600	Weak transcription	HSMM	muscle
30	chr9:13224000-13241400	Weak transcription	Ovary	ovary
31	chr9:13224000-13242200	Weak transcription	Fetal Stomach	stomach
32	chr9:13224000-13264600	Weak transcription	Osteobl	bone
33	chr9:13224200-13241800	Weak transcription	Fetal Muscle Leg	muscle
34	chr9:13224200-13245600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr9:13224400-13242600	Weak transcription	Fetal Lung	lung
36	chr9:13224400-13252400	Weak transcription	Liver	Liver
37	chr9:13224600-13231200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr9:13224600-13241800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr9:13224600-13242400	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr9:13224600-13247000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:13224800-13236600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:13225200-13236400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:13226000-13252800	Weak transcription	Fetal Heart	heart
44	chr9:13226200-13237000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr9:13226400-13247000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr9:13226600-13237200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:13226600-13242600	Weak transcription	Left Ventricle	heart
48	chr9:13226600-13259200	Weak transcription	Right Ventricle	heart
49	chr9:13226800-13278000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr9:13229200-13230200	Enhancers	HUES48 Cell Line	embryonic stem cell

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