Variant report

Variant	nsv892584
Chromosome Location	chr9:13214871-13350478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:837)
CpG islands
(count:672)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:837 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:13268423-13268869	K562	blood:	n/a	n/a
2	ARID3A	chr9:13269505-13269999	K562	blood:	n/a	n/a
3	ARID3A	chr9:13267952-13268141	K562	blood:	n/a	n/a
4	ATF1	chr9:13278032-13278621	K562	blood:	n/a	n/a
5	ATF1	chr9:13268465-13268833	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	chr9:13278144-13278639	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr9:13315456-13315474	K562	blood:	n/a	n/a
11	BHLHE40	chr9:13279384-13279648	K562	blood:	n/a	n/a
12	BHLHE40	chr9:13278045-13278680	K562	blood:	n/a	n/a
13	CBX3	chr9:13268543-13268820	K562	blood:	n/a	n/a
14	CCNT2	chr9:13278210-13278873	K562	blood:	n/a	n/a
15	CCNT2	chr9:13279271-13279892	K562	blood:	n/a	chr9:13279622-13279631
16	CEBPB	chr9:13219674-13220067	HepG2	liver:	n/a	chr9:13219944-13219955
17	CEBPB	chr9:13226944-13227262	HepG2	liver:	n/a	chr9:13227118-13227129 chr9:13227118-13227131 chr9:13227195-13227207
18	CEBPB	chr9:13219830-13220061	A549	lung:	n/a	chr9:13219944-13219955
19	CEBPB	chr9:13235169-13235395	A549	lung:	n/a	n/a
20	CEBPB	chr9:13267750-13268132	IMR90	lung:	n/a	chr9:13268032-13268045
21	CEBPB	chr9:13214924-13215198	HepG2	liver:	n/a	chr9:13215050-13215061
22	CEBPB	chr9:13261370-13261575	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:13219866-13220096	K562	blood:	n/a	chr9:13219944-13219955
24	CEBPB	chr9:13219778-13220078	IMR90	lung:	n/a	chr9:13219944-13219955
25	CEBPB	chr9:13226942-13227210	A549	lung:	n/a	chr9:13227118-13227129 chr9:13227118-13227131 chr9:13227195-13227207
26	CEBPB	chr9:13226855-13227285	IMR90	lung:	n/a	chr9:13227118-13227129 chr9:13227118-13227131 chr9:13227195-13227207
27	CEBPB	chr9:13274909-13275601	IMR90	lung:	n/a	n/a
28	CEBPD	chr9:13279233-13279576	HepG2	liver:	n/a	n/a
29	CEBPD	chr9:13268451-13268876	K562	blood:	n/a	n/a
30	CHD2	chr9:13279406-13279700	HepG2	liver:	n/a	n/a
31	CHD2	chr9:13279436-13279848	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr9:13279452-13279788	K562	blood:	n/a	n/a
33	CHD2	chr9:13278431-13278782	H1-hESC	embryonic stem cell:	n/a	chr9:13278434-13278444
34	CHD2	chr9:13278750-13278753	HepG2	liver:	n/a	n/a
35	CHD2	chr9:13279455-13279700	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr9:13278371-13278850	A549	lung:	n/a	n/a
37	CREB1	chr9:13277932-13278478	K562	blood:	n/a	chr9:13278215-13278228
38	CREB1	chr9:13279395-13279883	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr9:13279298-13279841	A549	lung:	n/a	n/a
40	CREB1	chr9:13279252-13279948	HepG2	liver:	n/a	n/a
41	CTBP2	chr9:13278130-13279032	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr9:13291860-13292010	GM12872	blood:	n/a	n/a
43	CTCF	chr9:13275521-13275605	GM20000	blood:	n/a	n/a
44	CTCF	chr9:13278400-13278550	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr9:13278820-13278970	A549	lung:	n/a	chr9:13278914-13278927 chr9:13278884-13278897
46	CTCF	chr9:13278800-13278950	HPF	lung:	n/a	chr9:13278914-13278927 chr9:13278884-13278897
47	CTCF	chr9:13291740-13291890	HCFaa	heart:	n/a	n/a
48	CTCF	chr9:13278800-13278950	SK-N-SH_RA	brain:	n/a	chr9:13278914-13278927 chr9:13278884-13278897
49	CTCF	chr9:13278660-13278810	BE2_C	brain:	n/a	n/a
50	CTCF	chr9:13278780-13278930	NHDF-neo	bronchial:	n/a	chr9:13278914-13278927 chr9:13278884-13278897

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13323113-13323163	AG09319	gingival:	n/a
2	chr9:13323113-13323163	AG09319	gingival:	n/a
3	chr9:13323113-13323163	HCF	heart:	n/a
4	chr9:13278512-13278562	ECC-1	luminal epithelium:	n/a
5	chr9:13251228-13251278	MCF10A-Er-Src	breast:	n/a
6	chr9:13280025-13280075	GM12878	blood:	n/a
7	chr9:13249504-13249554	SAEC	small airway:	n/a
8	chr9:13279482-13279532	BJ	skin:	n/a
9	chr9:13284899-13284949	NB4	blood:	n/a
10	chr9:13284899-13284949	HepG2	liver:	n/a
11	chr9:13323113-13323163	PANC-1	pancreas:	n/a
12	chr9:13279482-13279532	GM06990	blood:	n/a
13	chr9:13279482-13279532	HIPEpiC	eye:	n/a
14	chr9:13249504-13249554	PFSK-1	brain:	n/a
15	chr9:13278977-13279027	RPTEC	kidney:	n/a
16	chr9:13251431-13251481	PANC-1	pancreas:	n/a
17	chr9:13249504-13249554	Jurkat	blood:	n/a
18	chr9:13323113-13323163	HPAEpiC	pulmonary alveolar:	n/a
19	chr9:13278512-13278562	AG04449	skin:	fetal
20	chr9:13284899-13284949	NH-A	brain:	n/a
21	chr9:13251228-13251278	H1-hESC	embryonic stem cell:	embryo
22	chr9:13280025-13280075	AG04450	lung:	fetal
23	chr9:13280025-13280075	NT2-D1	testis:	n/a
24	chr9:13251431-13251481	BE2_C	brain:	n/a
25	chr9:13249504-13249554	GM06990	blood:	n/a
26	chr9:13284899-13284949	MCF-7	breast:	n/a
27	chr9:13323130-13323180	Jurkat	blood:	n/a
28	chr9:13323130-13323180	HepG2	liver:	n/a
29	chr9:13279482-13279532	HUVEC	blood vessel:	n/a
30	chr9:13278977-13279027	NHBE	bronchial:	n/a
31	chr9:13251431-13251481	SK-N-SH	brain:	n/a
32	chr9:13279482-13279532	Jurkat	blood:	n/a
33	chr9:13278977-13279027	T-47D	breast:	n/a
34	chr9:13251228-13251278	Hepatocyte	liver:	n/a
35	chr9:13249504-13249554	MCF10A-Er-Src	breast:	n/a
36	chr9:13251228-13251278	NHBE	bronchial:	n/a
37	chr9:13278512-13278562	SAEC	small airway:	n/a
38	chr9:13278626-13278676	AG09319	gingival:	n/a
39	chr9:13249504-13249554	H1-hESC	embryonic stem cell:	embryo
40	chr9:13251228-13251278	U87	brain:	n/a
41	chr9:13323130-13323180	H1-hESC	embryonic stem cell:	embryo
42	chr9:13251228-13251278	SK-N-SH	brain:	n/a
43	chr9:13279482-13279532	PFSK-1	brain:	n/a
44	chr9:13251431-13251481	NB4	blood:	n/a
45	chr9:13278626-13278676	HMEC	breast:	n/a
46	chr9:13278977-13279027	HRCEpiC	kidney:	n/a
47	chr9:13323113-13323163	Caco-2	colon:	n/a
48	chr9:13278626-13278676	ovcar-3	ovarian:	n/a
49	chr9:13278512-13278562	AG09319	gingival:	n/a
50	chr9:13278626-13278676	Caco-2	colon:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:13227295..13229314-chr9:13231919..13233666,2	K562	blood:
2	chr9:13256063..13258580-chr9:13259796..13261728,2	MCF-7	breast:
3	chr9:13033734..13035793-chr9:13280439..13283221,2	K562	blood:
4	chr9:13257934..13260781-chr9:13265128..13267553,2	K562	blood:
5	chr9:13236159..13239673-chr9:13240021..13241602,3	K562	blood:
6	chr9:13253272..13256171-chr9:13277669..13280982,3	MCF-7	breast:
7	chr9:13245657..13247575-chr9:13257459..13259209,2	MCF-7	breast:
8	chr17:55977919..55980808-chr9:13278471..13279995,2	MCF-7	breast:
9	chr9:13266586..13268806-chr9:13275605..13278055,2	MCF-7	breast:
10	chr9:13266586..13268806-chr9:13275605..13278055,2	MCF-7	breast:
11	chr9:13287399..13289604-chr9:13290158..13292995,2	K562	blood:
12	chr9:13287399..13289604-chr9:13290158..13292995,2	K562	blood:
13	chr9:13230183..13232341-chr9:13234177..13235807,2	MCF-7	breast:
14	chr9:13223131..13225371-chr9:13226892..13228609,2	K562	blood:
15	chr9:13275549..13278427-chr9:13279998..13281670,2	K562	blood:
16	chr9:13276562..13283255-chr9:13284283..13286656,6	MCF-7	breast:
17	chr9:13278476..13280409-chr9:13296744..13299210,3	MCF-7	breast:
18	chr9:13223131..13225371-chr9:13226892..13228609,2	K562	blood:
19	chr9:13267404..13273261-chr9:13274037..13279578,8	K562	blood:
20	chr9:13227295..13229314-chr9:13231919..13233666,2	K562	blood:
21	chr9:13236159..13239673-chr9:13240021..13241602,3	K562	blood:
22	chr9:13256063..13258580-chr9:13259796..13261728,2	MCF-7	breast:
23	chr9:13261386..13263235-chr9:13277146..13279520,2	MCF-7	breast:
24	chr9:13257934..13260781-chr9:13265128..13267553,2	K562	blood:
25	chr9:13278089..13282078-chr9:14313109..14316114,3	MCF-7	breast:
26	chr9:13245657..13247575-chr9:13257459..13259209,2	MCF-7	breast:
27	chr9:13281407..13283656-chr9:13286644..13288961,2	MCF-7	breast:
28	chr9:13275549..13278427-chr9:13279998..13281670,2	K562	blood:
29	chr9:13230183..13232341-chr9:13234177..13235807,2	MCF-7	breast:
30	chr9:13266536..13270627-chr9:13277145..13281714,5	K562	blood:
31	chr9:13278596..13280107-chr9:13281623..13284453,2	MCF-7	breast:
32	chr9:13277467..13280147-chr9:13286399..13289258,3	MCF-7	breast:
33	chr9:13281407..13283656-chr9:13286644..13288961,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 4482 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4482 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17273416	chr9:13214871-13214872	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375222006	chr9:13214879-13214880	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116525551	chr9:13214888-13214889	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188747201	chr9:13214894-13214895	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141721694	chr9:13214958-13214959	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117557763	chr9:13215016-13215017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192345029	chr9:13215027-13215028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543482066	chr9:13215029-13215030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549254540	chr9:13215033-13215034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116068734	chr9:13215034-13215035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576759948	chr9:13215049-13215050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534771931	chr9:13215088-13215089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562774817	chr9:13215102-13215103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114568111	chr9:13215108-13215109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35620137	chr9:13215119-13215120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145988382	chr9:13215144-13215145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs71507368	chr9:13215208-13215209	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs576318022	chr9:13215254-13215255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562280502	chr9:13215325-13215326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183247560	chr9:13215343-13215344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542512704	chr9:13215381-13215382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141428507	chr9:13215437-13215438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575759730	chr9:13215438-13215439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138863553	chr9:13215445-13215446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs55720256	chr9:13215453-13215454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142869684	chr9:13215466-13215467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147443505	chr9:13215475-13215476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72706374	chr9:13215482-13215483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564094375	chr9:13215511-13215512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62532869	chr9:13215519-13215520	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs549571958	chr9:13215528-13215529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563302168	chr9:13215553-13215554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528851916	chr9:13215560-13215561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71507369	chr9:13215578-13215579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549311423	chr9:13215602-13215603	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566012182	chr9:13215604-13215605	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191665406	chr9:13215695-13215696	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71507370	chr9:13215741-13215742	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372869059	chr9:13215752-13215753	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138456434	chr9:13215753-13215754	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201749654	chr9:13215761-13215762	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549903049	chr9:13215763-13215764	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56281339	chr9:13215773-13215774	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9697033	chr9:13215774-13215775	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7045678	chr9:13215775-13215776	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371975205	chr9:13215776-13215777	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7045679	chr9:13215777-13215778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551647120	chr9:13215799-13215800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150559904	chr9:13215801-13215802	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571342638	chr9:13215808-13215809	Strong transcription 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
Breast cancer	21611746	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1325 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13121600-13225200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr9:13135400-13223600	Weak transcription	Lung	lung
3	chr9:13145400-13228600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr9:13164200-13248600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr9:13164200-13258800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:13182200-13226800	Weak transcription	Fetal Brain Male	brain
7	chr9:13188000-13220800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:13189000-13221000	Weak transcription	NHLF	lung
9	chr9:13189000-13268600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:13190400-13237800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:13195400-13223400	Weak transcription	Fetal Stomach	stomach
12	chr9:13202800-13215600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr9:13202800-13220800	Weak transcription	Placenta	Placenta
14	chr9:13202800-13226400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr9:13202800-13250600	Weak transcription	Pancreas	Pancrea
16	chr9:13202800-13250800	Weak transcription	Psoas Muscle	Psoas
17	chr9:13203000-13223600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr9:13203000-13224800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr9:13203000-13225400	Weak transcription	Brain Anterior Caudate	brain
20	chr9:13203000-13261000	Weak transcription	Colon Smooth Muscle	Colon
21	chr9:13203400-13223600	Weak transcription	Ovary	ovary
22	chr9:13203400-13224800	Weak transcription	Rectal Smooth Muscle	rectum
23	chr9:13203400-13226400	Weak transcription	Right Ventricle	heart
24	chr9:13203400-13247000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr9:13203600-13216200	Weak transcription	Brain Substantia Nigra	brain
26	chr9:13203600-13219600	Weak transcription	HSMMtube	muscle
27	chr9:13203600-13245600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr9:13203800-13220800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:13204000-13215000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr9:13204000-13241800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr9:13204000-13249200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:13204200-13244600	Weak transcription	HepG2	liver
33	chr9:13204400-13221800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr9:13206000-13218800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr9:13206000-13219400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr9:13206000-13223000	Weak transcription	Brain Hippocampus Middle	brain
37	chr9:13206000-13229200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr9:13206000-13247000	Weak transcription	Brain Angular Gyrus	brain
39	chr9:13206200-13216200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr9:13206400-13216000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr9:13206400-13216000	Weak transcription	Osteobl	bone
42	chr9:13206400-13216600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:13206400-13219400	Weak transcription	Liver	Liver
44	chr9:13206600-13216400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr9:13207600-13228200	Weak transcription	Esophagus	oesophagus
46	chr9:13208200-13265000	Weak transcription	Aorta	Aorta
47	chr9:13209200-13216400	Weak transcription	Adipose Nuclei	Adipose
48	chr9:13209800-13215000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:13209800-13266000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr9:13211000-13225200	Weak transcription	Fetal Intestine Large	intestine

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