Variant report

Variant	nsv471290
Chromosome Location	chr9:21694038-21721939
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	chr9:21709533-21709820	HepG2	liver:	n/a	n/a
2	BATF	chr9:21711502-21711771	GM12878	blood:	n/a	chr9:21711661-21711672
3	BATF	chr9:21711462-21711794	GM12878	blood:	n/a	chr9:21711661-21711672
4	CBX3	chr9:21709389-21709975	HCT-116	colon:	n/a	n/a
5	CEBPB	chr9:21702033-21702278	A549	lung:	n/a	chr9:21702179-21702190 chr9:21702179-21702188
6	CEBPB	chr9:21711413-21712016	HCT-116	colon:	n/a	n/a
7	CEBPB	chr9:21702010-21702303	IMR90	lung:	n/a	chr9:21702179-21702190 chr9:21702179-21702188
8	CEBPB	chr9:21711549-21711834	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:21715538-21715759	IMR90	lung:	n/a	n/a
10	CHD1	chr9:21711966-21712002	GM12878	blood:	n/a	n/a
11	CHD2	chr9:21696622-21696802	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr9:21709530-21709809	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr9:21696745-21696883	MCF-7	breast:	n/a	n/a
14	CTCF	chr9:21709580-21709730	HFF	foreskin:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
15	CTCF	chr9:21709300-21709450	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr9:21696725-21696900	MCF-7	breast:	n/a	n/a
17	CTCF	chr9:21696808-21696829	Medullo	brain:	n/a	n/a
18	CTCF	chr9:21709434-21709878	A549	lung:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
19	CTCF	chr9:21709093-21709992	A549	lung:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
20	CTCF	chr9:21709535-21709787	LNCaP	prostate:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
21	CTCF	chr9:21708800-21708950	GM12865	blood:	n/a	n/a
22	CTCF	chr9:21709538-21709782	GM13977	blood:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
23	CTCF	chr9:21710560-21710710	HMF	breast:	n/a	n/a
24	CTCF	chr9:21696760-21696910	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr9:21696700-21696850	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr9:21696660-21696810	GM12875	blood:	n/a	n/a
27	CTCF	chr9:21709560-21709710	GM12873	blood:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
28	CTCF	chr9:21709580-21709730	HCPEpiC	choroid plexus:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
29	CTCF	chr9:21696680-21696830	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr9:21708880-21709030	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr9:21709520-21709670	GM12870	blood:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669
32	CTCF	chr9:21696720-21696870	AG04449	skin:	n/a	n/a
33	CTCF	chr9:21709600-21709750	HUVEC	blood vessel:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
34	CTCF	chr9:21709524-21709716	T-47D	breast:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
35	CTCF	chr9:21696760-21696910	HCM	heart:	n/a	n/a
36	CTCF	chr9:21709600-21709750	MCF-7	breast:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
37	CTCF	chr9:21709580-21709730	HFF-Myc	foreskin:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
38	CTCF	chr9:21709509-21709762	Kidney_OC	kidney:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
39	CTCF	chr9:21709539-21709768	MCF-7	breast:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
40	CTCF	chr9:21709520-21709670	GM12864	blood:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669
41	CTCF	chr9:21709580-21709730	HCT-116	colon:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
42	CTCF	chr9:21709600-21709750	HRPEpiC	eye:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
43	CTCF	chr9:21696696-21696919	A549	lung:	n/a	n/a
44	CTCF	chr9:21696758-21696839	NHEK	skin:	n/a	n/a
45	CTCF	chr9:21696700-21696850	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr9:21709540-21709769	HepG2	liver:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
47	CTCF	chr9:21709920-21710070	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr9:21709560-21709710	HPAF	blood vessel:	n/a	chr9:21709652-21709670 chr9:21709657-21709665 chr9:21709653-21709669 chr9:21709654-21709675
49	CTCF	chr9:21709120-21709270	AG09319	gingival:	n/a	n/a
50	CTCF	chr9:21696698-21696917	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21696666-21696716	HNPCEpiC	eye:	n/a
2	chr9:21696666-21696716	NB4	blood:	n/a
3	chr9:21696666-21696716	GM06990	blood:	n/a
4	chr9:21696666-21696716	HCF	heart:	n/a
5	chr9:21696666-21696716	HCPEpiC	choroid plexus:	n/a
6	chr9:21696666-21696716	U87	brain:	n/a
7	chr9:21696666-21696716	MCF-7	breast:	n/a
8	chr9:21696666-21696716	BE2_C	brain:	n/a
9	chr9:21696666-21696716	ProgFib	skin:	n/a
10	chr9:21696666-21696716	HRPEpiC	eye:	n/a
11	chr9:21696666-21696716	MCF10A-Er-Src	breast:	n/a
12	chr9:21696666-21696716	NHDF-neo	bronchial:	n/a
13	chr9:21696666-21696716	HMEC	breast:	n/a
14	chr9:21696666-21696716	GM12892	blood:	n/a
15	chr9:21696666-21696716	Caco-2	colon:	n/a
16	chr9:21696666-21696716	PFSK-1	brain:	n/a
17	chr9:21696666-21696716	HAEpiC	amniotic membrane:	n/a
18	chr9:21696666-21696716	Jurkat	blood:	n/a
19	chr9:21696666-21696716	HUVEC	blood vessel:	n/a
20	chr9:21696666-21696716	HEK293	kidney:	embryo
21	chr9:21696666-21696716	CMK	blood:	n/a
22	chr9:21696666-21696716	LNCaP	prostate:	n/a
23	chr9:21696666-21696716	HepG2	liver:	n/a
24	chr9:21696666-21696716	ovcar-3	ovarian:	n/a
25	chr9:21696666-21696716	HIPEpiC	eye:	n/a
26	chr9:21696666-21696716	HL-60	blood:	n/a
27	chr9:21696666-21696716	HRCEpiC	kidney:	n/a
28	chr9:21696666-21696716	GM12878	blood:	n/a
29	chr9:21696666-21696716	SK-N-MC	brain:	n/a
30	chr9:21696666-21696716	NHBE	bronchial:	n/a
31	chr9:21696666-21696716	T-47D	breast:	n/a
32	chr9:21696666-21696716	A549	lung:	n/a
33	chr9:21696666-21696716	H1-hESC	embryonic stem cell:	embryo
34	chr9:21696666-21696716	HRE	kidney:	n/a
35	chr9:21696666-21696716	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:21696666-21696716	HCT-116	colon:	n/a
37	chr9:21696666-21696716	SK-N-SH	brain:	n/a
38	chr9:21696666-21696716	IMR90	lung:	fetal
39	chr9:21696666-21696716	Hepatocyte	liver:	n/a
40	chr9:21696666-21696716	RPTEC	kidney:	n/a
41	chr9:21696666-21696716	Hela-S3	cervix:	n/a
42	chr9:21696666-21696716	NT2-D1	testis:	n/a
43	chr9:21696666-21696716	K562	blood:	n/a
44	chr9:21696666-21696716	GM12891	blood:	n/a
45	chr9:21696666-21696716	SK-N-SH_RA	brain:	n/a
46	chr9:21696666-21696716	AG09319	gingival:	n/a
47	chr9:21696666-21696716	NH-A	brain:	n/a
48	chr9:21696666-21696716	PrEC	prostate:	n/a
49	chr9:21696666-21696716	SKMC	muscle:	n/a
50	chr9:21696666-21696716	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:21709315..21710109-chr9:21789136..21789898,2	MCF-7	breast:
2	chr9:21709125..21709738-chr9:21789173..21789997,3	MCF-7	breast:
3	chr9:21681458..21682986-chr9:21704343..21706212,2	MCF-7	breast:
4	chr11:93474769..93475337-chr9:21707894..21708478,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTAP-5	chr9:21699313-21699569	NONHSAT130395

Variant related genes	Relation type
KHSRPP1	TF binding region
RN7SL151P	TF binding region
KHSRPP1	CpG island
RN7SL151P	CpG island
ENSG00000182919	chromatin interactions
ENSG00000166012	chromatin interactions

Extended variants
information (count: 1269 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2123338	chr9:21694039-21694040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547217701	chr9:21694084-21694085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567846550	chr9:21694109-21694110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144676187	chr9:21694126-21694127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550359662	chr9:21694167-21694168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12003470	chr9:21694178-21694179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs538970746	chr9:21694189-21694190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117979077	chr9:21694215-21694216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113024207	chr9:21694222-21694223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535027803	chr9:21694247-21694248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183964453	chr9:21694330-21694331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553584547	chr9:21694349-21694350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572142886	chr9:21694353-21694354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373296274	chr9:21694365-21694366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115871783	chr9:21694374-21694375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571038473	chr9:21694387-21694388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574876982	chr9:21694427-21694428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542415076	chr9:21694474-21694475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562687762	chr9:21694497-21694498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189430924	chr9:21694501-21694502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545349718	chr9:21694550-21694551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564856928	chr9:21694588-21694589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6475547	chr9:21694602-21694603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542006637	chr9:21694605-21694606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560781986	chr9:21694607-21694608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138162604	chr9:21694612-21694613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575708059	chr9:21694625-21694626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550081291	chr9:21694653-21694654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569946705	chr9:21694657-21694658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6475548	chr9:21694664-21694665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs551300134	chr9:21694677-21694678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552494947	chr9:21694687-21694688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539517452	chr9:21694693-21694694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117202803	chr9:21694702-21694703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564745870	chr9:21694703-21694704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148518379	chr9:21694723-21694724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142862784	chr9:21694731-21694732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568424682	chr9:21694743-21694744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537573491	chr9:21694762-21694763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146586025	chr9:21694775-21694776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576338341	chr9:21694781-21694782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545321048	chr9:21694821-21694822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181950559	chr9:21694844-21694845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572314559	chr9:21694847-21694848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185982249	chr9:21694866-21694867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569618212	chr9:21694879-21694880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79365815	chr9:21694885-21694886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190047384	chr9:21694904-21694905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543149927	chr9:21694954-21694955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141306403	chr9:21694970-21694971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:155)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	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
Chronic myeloid leukemia	21384125	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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Barrett''s syndrome	19417022	CNVD
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21685200-21695600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:21688400-21696200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:21690600-21701200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:21691000-21695400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:21691600-21695400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:21695400-21696600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:21695400-21696800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:21695600-21696600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:21695800-21696600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:21696200-21696400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr9:21696200-21696600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:21696400-21696600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:21696400-21697000	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr9:21696400-21697200	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr9:21696600-21696800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:21696600-21697000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr9:21696600-21697000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:21696600-21697000	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr9:21696600-21707000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:21696800-21697000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr9:21696800-21697000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr9:21699600-21707600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:21699800-21700400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr9:21701200-21701400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:21706800-21708600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr9:21707000-21708800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr9:21707200-21708400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr9:21707200-21712200	Enhancers	HMEC	breast
29	chr9:21707600-21710000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:21707600-21711000	Enhancers	NHEK	skin
31	chr9:21708000-21709600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr9:21708200-21708600	Enhancers	HSMM	muscle
33	chr9:21708200-21709200	Enhancers	Fetal Stomach	stomach
34	chr9:21708200-21709200	Enhancers	NHDF-Ad	bronchial
35	chr9:21708200-21709400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:21708200-21709400	Enhancers	HSMMtube	muscle
37	chr9:21708400-21708800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr9:21708400-21709200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:21708400-21709200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr9:21708400-21709600	Enhancers	A549	lung
41	chr9:21708400-21709600	Enhancers	Osteobl	bone
42	chr9:21708400-21713000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr9:21708600-21708800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr9:21708600-21709000	Flanking Active TSS	HSMM	muscle
45	chr9:21708800-21709000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr9:21708800-21709000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:21708800-21709000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:21708800-21710600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr9:21709000-21709200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:21709000-21709200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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