Variant report

Variant	nsv1015898
Chromosome Location	chr9:8753534-9011443
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	ARID3A	chr9:8868744-8869021	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:8961022-8961768	HepG2	liver:	n/a	n/a
3	ATF2	chr9:8858467-8859172	H1-hESC	embryonic stem cell:	n/a	chr9:8858876-8858890 chr9:8858878-8858889
4	ATF2	chr9:8858576-8859063	H1-hESC	embryonic stem cell:	n/a	chr9:8858876-8858890 chr9:8858878-8858889
5	BCL11A	chr9:8868710-8869028	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:8895967-8895969	A549	lung:	n/a	n/a
7	BHLHE40	chr9:8961130-8961628	HepG2	liver:	n/a	n/a
8	BRCA1	chr9:8855216-8855273	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr9:8961431-8961631	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:8910638-8910923	IMR90	lung:	n/a	n/a
11	CEBPB	chr9:8961081-8961810	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:8782267-8782532	H1-hESC	embryonic stem cell:	n/a	chr9:8782419-8782430
13	CEBPB	chr9:8889121-8889489	IMR90	lung:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
14	CEBPB	chr9:8863911-8864232	H1-hESC	embryonic stem cell:	n/a	chr9:8864067-8864078 chr9:8864066-8864079
15	CEBPB	chr9:8987639-8987844	H1-hESC	embryonic stem cell:	n/a	chr9:8987749-8987758 chr9:8987747-8987758 chr9:8987747-8987760
16	CEBPB	chr9:8961188-8961617	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:8765144-8765459	A549	lung:	n/a	chr9:8765314-8765325
18	CEBPB	chr9:8990081-8990286	A549	lung:	n/a	chr9:8990232-8990245 chr9:8990232-8990243
19	CEBPB	chr9:8910663-8910909	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:9010854-9010971	H1-hESC	embryonic stem cell:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
21	CEBPB	chr9:8815292-8815726	HepG2	liver:	n/a	chr9:8815612-8815625
22	CEBPB	chr9:8889203-8889415	K562	blood:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
23	CEBPB	chr9:9010826-9010992	K562	blood:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
24	CEBPB	chr9:9010741-9010996	A549	lung:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
25	CEBPB	chr9:8889133-8889482	HepG2	liver:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
26	CEBPB	chr9:8791919-8792041	A549	lung:	n/a	n/a
27	CEBPB	chr9:8765139-8765438	HepG2	liver:	n/a	chr9:8765314-8765325
28	CEBPB	chr9:8961184-8961759	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:8862492-8862809	A549	lung:	n/a	chr9:8862647-8862660 chr9:8862648-8862659 chr9:8862649-8862658 chr9:8862647-8862658 chr9:8862647-8862660
30	CEBPB	chr9:8864000-8864208	HepG2	liver:	n/a	chr9:8864067-8864078 chr9:8864066-8864079
31	CEBPB	chr9:8782263-8782583	HepG2	liver:	n/a	chr9:8782419-8782430
32	CEBPB	chr9:8833481-8833697	K562	blood:	n/a	chr9:8833624-8833637 chr9:8833625-8833636 chr9:8833624-8833637 chr9:8833624-8833637
33	CEBPB	chr9:8765187-8765410	K562	blood:	n/a	chr9:8765314-8765325
34	CEBPB	chr9:8858706-8858888	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr9:8992944-8993144	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:9006505-9006741	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:8945985-8946238	HepG2	liver:	n/a	chr9:8946106-8946117
38	CEBPB	chr9:8862470-8862814	HepG2	liver:	n/a	chr9:8862647-8862660 chr9:8862648-8862659 chr9:8862649-8862658 chr9:8862647-8862658 chr9:8862647-8862660
39	CEBPB	chr9:8782264-8782608	IMR90	lung:	n/a	chr9:8782419-8782430
40	CEBPB	chr9:8765147-8765485	IMR90	lung:	n/a	chr9:8765314-8765325
41	CEBPB	chr9:8889126-8889470	H1-hESC	embryonic stem cell:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
42	CEBPB	chr9:8990077-8990402	HepG2	liver:	n/a	chr9:8990232-8990245 chr9:8990232-8990243
43	CEBPB	chr9:8774371-8774528	A549	lung:	n/a	n/a
44	CEBPB	chr9:8782348-8782559	K562	blood:	n/a	chr9:8782419-8782430
45	CEBPB	chr9:8926156-8926446	HepG2	liver:	n/a	chr9:8926304-8926313 chr9:8926302-8926313 chr9:8926304-8926315
46	CEBPB	chr9:9010710-9011045	IMR90	lung:	n/a	chr9:9010892-9010905 chr9:9010894-9010903 chr9:9010892-9010903
47	CEBPB	chr9:8775818-8775879	K562	blood:	n/a	chr9:8775851-8775862
48	CEBPB	chr9:8946121-8946175	A549	lung:	n/a	n/a
49	CEBPB	chr9:8889118-8889488	A549	lung:	n/a	chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889298-8889307 chr9:8889296-8889307
50	CEBPB	chr9:8899331-8899567	HepG2	liver:	n/a	chr9:8899382-8899391 chr9:8899380-8899391 chr9:8899382-8899393

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:8858259-8858309	BE2_C	brain:	n/a
2	chr9:8857502-8857552	AoSMC	blood vessel:	n/a
3	chr9:8858644-8858694	CMK	blood:	n/a
4	chr9:8858259-8858309	NT2-D1	testis:	n/a
5	chr9:8858259-8858309	BJ	skin:	n/a
6	chr9:8852055-8852105	HCM	heart:	n/a
7	chr9:8835149-8835199	HRE	kidney:	n/a
8	chr9:8852055-8852105	SKMC	muscle:	n/a
9	chr9:8858574-8858624	LNCaP	prostate:	n/a
10	chr9:8857502-8857552	HAEpiC	amniotic membrane:	n/a
11	chr9:8858574-8858624	SK-N-SH_RA	brain:	n/a
12	chr9:8856695-8856745	GM12891	blood:	n/a
13	chr9:8852055-8852105	AG09319	gingival:	n/a
14	chr9:8835149-8835199	Caco-2	colon:	n/a
15	chr9:8835149-8835199	H1-hESC	embryonic stem cell:	embryo
16	chr9:8858259-8858309	NHBE	bronchial:	n/a
17	chr9:8835149-8835199	NB4	blood:	n/a
18	chr9:8858644-8858694	T-47D	breast:	n/a
19	chr9:8857486-8857536	PANC-1	pancreas:	n/a
20	chr9:8857486-8857536	HRE	kidney:	n/a
21	chr9:8857502-8857552	Jurkat	blood:	n/a
22	chr9:8856695-8856745	AG04450	lung:	fetal
23	chr9:8857491-8857541	SAEC	small airway:	n/a
24	chr9:8852055-8852105	ProgFib	skin:	n/a
25	chr9:8858644-8858694	HCT-116	colon:	n/a
26	chr9:8857491-8857541	T-47D	breast:	n/a
27	chr9:8857491-8857541	HepG2	liver:	n/a
28	chr9:8835149-8835199	HPAEpiC	pulmonary alveolar:	n/a
29	chr9:8857502-8857552	NT2-D1	testis:	n/a
30	chr9:8852055-8852105	NB4	blood:	n/a
31	chr9:8858644-8858694	GM12892	blood:	n/a
32	chr9:8858259-8858309	HepG2	liver:	n/a
33	chr9:8852055-8852105	SK-N-SH	brain:	n/a
34	chr9:8835149-8835199	GM12892	blood:	n/a
35	chr9:8857486-8857536	HUVEC	blood vessel:	n/a
36	chr9:8858644-8858694	ProgFib	skin:	n/a
37	chr9:8857491-8857541	Caco-2	colon:	n/a
38	chr9:8857502-8857552	HRE	kidney:	n/a
39	chr9:8858259-8858309	MCF-7	breast:	n/a
40	chr9:8857502-8857552	GM12892	blood:	n/a
41	chr9:8856695-8856745	HRE	kidney:	n/a
42	chr9:8852055-8852105	CMK	blood:	n/a
43	chr9:8858259-8858309	NB4	blood:	n/a
44	chr9:8858574-8858624	GM19239	blood:	n/a
45	chr9:8858644-8858694	HCM	heart:	n/a
46	chr9:8858259-8858309	U87	brain:	n/a
47	chr9:8857502-8857552	HRPEpiC	eye:	n/a
48	chr9:8858644-8858694	AG10803	skin:	n/a
49	chr9:8858644-8858694	Hela-S3	cervix:	n/a
50	chr9:8856695-8856745	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr9:8868603..8871582-chr9:8873717..8875264,2	K562	blood:
2	chr9:7569797..7570734-chr9:8895690..8896630,4	MCF-7	breast:
3	chr9:8485590..8486306-chr9:8895648..8896453,2	MCF-7	breast:
4	chr9:7844225..7844973-chr9:8895548..8896327,4	MCF-7	breast:
5	chr9:7569880..7570683-chr9:8895710..8896327,2	MCF-7	breast:
6	chr9:8868603..8871582-chr9:8873717..8875264,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-9	chr9:8962124-8962189	ENSG00000234021
2	lnc-KDM4C-9	chr9:8936079-8936179	ENSG00000234021
3	lnc-KDM4C-17	chr9:8849956-8851724	ucscGeneNc_uc003zku_1
4	lnc-KDM4C-8	chr9:8859956-8861724	ENSG00000225706
5	lnc-KDM4C-8	chr9:8860782-8862255	ENSG00000225706
6	lnc-KDM4C-9	chr9:8958722-8958848	ENSG00000234021
7	lnc-KDM4C-8	chr9:8858130-8858323	ENSG00000225706
8	lnc-KDM4C-17	chr9:8848134-8848323	ucscGeneNc_uc003zku_1
9	lnc-KDM4C-8	chr9:8858134-8858323	ENSG00000225706
10	lnc-KDM4C-9	chr9:8962800-8963077	ENSG00000234021

Variant related genes	Relation type
ENSG00000251699	TF binding region
RNU7-185P	TF binding region
PTPRD	TF binding region
ENSG00000234021	TF binding region
ENSG00000225706	TF binding region
ENSG00000251699	CpG island
RNU7-185P	CpG island
PTPRD	CpG island
ENSG00000234021	CpG island
ENSG00000225706	CpG island
ENSG00000153707	chromatin interactions
HNRNPK	miRNA target sites
PLEC	miRNA target sites
CCDC76	miRNA target sites
WHSC1L1	miRNA target sites

Extended variants
information (count: 10260 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:10260 , 50 per page) page: 1 2 3 4 5 6 7 ... 206

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7861848	chr9:8753534-8753535	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547262461	chr9:8753542-8753543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386732369	chr9:8753567-8753568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537626379	chr9:8753571-8753572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555700669	chr9:8753572-8753573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58121486	chr9:8753574-8753575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7033599	chr9:8753594-8753595	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs542567352	chr9:8753620-8753621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559430875	chr9:8753632-8753633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141080803	chr9:8753650-8753651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185332909	chr9:8753657-8753658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577657255	chr9:8753713-8753714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150094390	chr9:8753751-8753752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73419274	chr9:8753754-8753755	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530929128	chr9:8753755-8753756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4740961	chr9:8753803-8753804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73419275	chr9:8753828-8753829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551316356	chr9:8753864-8753865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528345638	chr9:8753866-8753867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs386732370	chr9:8753867-8753868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191827034	chr9:8753869-8753870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532177767	chr9:8753883-8753884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112057788	chr9:8753907-8753908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184096116	chr9:8753916-8753917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113233362	chr9:8753918-8753919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546656491	chr9:8753921-8753922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377003266	chr9:8753928-8753929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567810371	chr9:8753931-8753932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188388819	chr9:8753960-8753961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146955095	chr9:8753964-8753965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566459445	chr9:8753973-8753974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138156845	chr9:8753984-8753985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180863745	chr9:8753996-8753997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558072189	chr9:8754016-8754017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113708362	chr9:8754027-8754028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143109899	chr9:8754040-8754041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148276940	chr9:8754044-8754045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528335416	chr9:8754057-8754058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568971055	chr9:8754062-8754063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112172778	chr9:8754069-8754070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111796394	chr9:8754091-8754092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150622111	chr9:8754100-8754101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185712463	chr9:8754110-8754111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568763505	chr9:8754132-8754133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573569952	chr9:8754138-8754139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529796528	chr9:8754142-8754143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113062178	chr9:8754145-8754146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72702322	chr9:8754165-8754166	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190671254	chr9:8754172-8754173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534918193	chr9:8754208-8754209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	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
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
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Renal cell carcinoma	21215367	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

Chromatin state (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8750000-8760000	Weak transcription	Aorta	Aorta
2	chr9:8750400-8753600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:8751000-8757800	Weak transcription	Fetal Brain Male	brain
4	chr9:8751200-8758000	Weak transcription	Brain Substantia Nigra	brain
5	chr9:8751200-8764400	Weak transcription	Fetal Stomach	stomach
6	chr9:8751400-8754800	Weak transcription	Brain Germinal Matrix	brain
7	chr9:8752200-8754400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:8752200-8755800	Weak transcription	Brain Hippocampus Middle	brain
9	chr9:8752200-8757800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr9:8752200-8759800	Weak transcription	Brain Anterior Caudate	brain
11	chr9:8752200-8760600	Weak transcription	Brain Angular Gyrus	brain
12	chr9:8752200-8760800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr9:8752200-8776600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr9:8752800-8756000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr9:8752800-8756000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:8752800-8756200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr9:8752800-8758000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:8752800-8758000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:8752800-8760000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:8752800-8769400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:8753000-8759800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr9:8753200-8756400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:8753400-8761000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:8753600-8758000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr9:8754400-8755000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr9:8754800-8755200	Enhancers	Brain Germinal Matrix	brain
27	chr9:8755000-8755800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:8755800-8756000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:8755800-8756600	Enhancers	Brain Hippocampus Middle	brain
30	chr9:8756000-8756400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:8756000-8756400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr9:8756000-8756400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr9:8756200-8756600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr9:8756400-8757000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr9:8756400-8759400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:8756600-8760400	Weak transcription	Brain Hippocampus Middle	brain
37	chr9:8757000-8760400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr9:8757800-8758200	Enhancers	Fetal Brain Male	brain
39	chr9:8757800-8758200	Enhancers	Fetal Kidney	kidney
40	chr9:8757800-8758600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr9:8758000-8758200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:8758000-8758400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr9:8758000-8758400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:8758000-8758400	Enhancers	Brain Substantia Nigra	brain
45	chr9:8758200-8762600	Weak transcription	Fetal Kidney	kidney
46	chr9:8758200-8764000	Weak transcription	Fetal Brain Male	brain
47	chr9:8758400-8760600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr9:8758400-8761200	Weak transcription	Brain Substantia Nigra	brain
49	chr9:8758400-8763000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:8758600-8773200	Weak transcription	Brain Inferior Temporal Lobe	brain

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