Variant report

Variant	nsv876617
Chromosome Location	chr3:21955784-22310622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1351)
CpG islands
(count:183)
Chromatin interactive
region (count:34)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:22162549-22162915	HepG2	liver:	n/a	n/a
2	ATF1	chr3:22262669-22262674	K562	blood:	n/a	n/a
3	BACH1	chr3:22278430-22278679	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:22164137-22164374	GM12878	blood:	n/a	chr3:22164265-22164276
5	BATF	chr3:22278454-22278659	GM12878	blood:	n/a	chr3:22278545-22278556
6	BATF	chr3:22278419-22278711	GM12878	blood:	n/a	chr3:22278545-22278556
7	BATF	chr3:22164128-22164369	GM12878	blood:	n/a	chr3:22164265-22164276
8	BCL3	chr3:22272575-22272895	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:22261633-22261739	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:22159425-22159426	K562	blood:	n/a	n/a
11	BHLHE40	chr3:22159971-22159994	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:22130865-22131163	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:22164062-22164443	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:22147560-22148537	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr3:22258598-22258798	K562	blood:	n/a	n/a
16	CEBPB	chr3:22030956-22031213	A549	lung:	n/a	chr3:22031068-22031085 chr3:22031049-22031060
17	CEBPB	chr3:22298812-22299012	H1-hESC	embryonic stem cell:	n/a	chr3:22298928-22298939
18	CEBPB	chr3:22053597-22053883	A549	lung:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
19	CEBPB	chr3:22286635-22286817	A549	lung:	n/a	chr3:22286695-22286708 chr3:22286697-22286708
20	CEBPB	chr3:22200864-22201215	Hela-S3	cervix:	n/a	chr3:22201008-22201021
21	CEBPB	chr3:22137588-22137831	A549	lung:	n/a	chr3:22137755-22137766
22	CEBPB	chr3:22252947-22253151	A549	lung:	n/a	n/a
23	CEBPB	chr3:22286475-22286973	Hela-S3	cervix:	n/a	chr3:22286899-22286916 chr3:22286695-22286708 chr3:22286697-22286708
24	CEBPB	chr3:22298761-22299071	HepG2	liver:	n/a	chr3:22298928-22298939
25	CEBPB	chr3:22030829-22031267	Hela-S3	cervix:	n/a	chr3:22031068-22031085 chr3:22031049-22031060
26	CEBPB	chr3:22200829-22201208	HepG2	liver:	n/a	chr3:22201008-22201021
27	CEBPB	chr3:22137582-22137905	IMR90	lung:	n/a	chr3:22137755-22137766
28	CEBPB	chr3:22237586-22237702	A549	lung:	n/a	n/a
29	CEBPB	chr3:22298793-22299012	K562	blood:	n/a	chr3:22298928-22298939
30	CEBPB	chr3:22038239-22038536	A549	lung:	n/a	chr3:22038377-22038388
31	CEBPB	chr3:22038225-22038503	IMR90	lung:	n/a	chr3:22038377-22038388
32	CEBPB	chr3:22273501-22273834	HepG2	liver:	n/a	chr3:22273665-22273676
33	CEBPB	chr3:22159289-22159588	K562	blood:	n/a	n/a
34	CEBPB	chr3:22273512-22273819	IMR90	lung:	n/a	chr3:22273665-22273676
35	CEBPB	chr3:22298742-22299047	Hela-S3	cervix:	n/a	chr3:22298928-22298939
36	CEBPB	chr3:21955980-21956311	IMR90	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
37	CEBPB	chr3:22048817-22049249	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:22150505-22150716	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:22048834-22049295	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:21955973-21956275	HepG2	liver:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
41	CEBPB	chr3:22038218-22038531	HepG2	liver:	n/a	chr3:22038377-22038388
42	CEBPB	chr3:22162691-22163152	HepG2	liver:	n/a	chr3:22163128-22163139
43	CEBPB	chr3:22298770-22299053	A549	lung:	n/a	chr3:22298928-22298939
44	CEBPB	chr3:22053532-22054406	Hela-S3	cervix:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
45	CEBPB	chr3:21955978-21956313	Hela-S3	cervix:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
46	CEBPB	chr3:21996174-21996533	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:22148135-22148381	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr3:22053569-22053879	K562	blood:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
49	CEBPB	chr3:21956051-21956262	A549	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
50	CEBPB	chr3:21961843-21962449	IMR90	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22192127-22192177	IMR90	lung:	fetal
2	chr3:21960904-21960954	GM12891	blood:	n/a
3	chr3:22192127-22192177	PANC-1	pancreas:	n/a
4	chr3:22030381-22030431	T-47D	breast:	n/a
5	chr3:22030381-22030431	SK-N-SH	brain:	n/a
6	chr3:21960904-21960954	NT2-D1	testis:	n/a
7	chr3:21960904-21960954	AG09319	gingival:	n/a
8	chr3:21960904-21960954	PFSK-1	brain:	n/a
9	chr3:22192127-22192177	RPTEC	kidney:	n/a
10	chr3:22192127-22192177	Jurkat	blood:	n/a
11	chr3:22030381-22030431	NH-A	brain:	n/a
12	chr3:21960904-21960954	BE2_C	brain:	n/a
13	chr3:21960904-21960954	SKMC	muscle:	n/a
14	chr3:21960904-21960954	PANC-1	pancreas:	n/a
15	chr3:22030381-22030431	MCF-7	breast:	n/a
16	chr3:22192127-22192177	AG09319	gingival:	n/a
17	chr3:21960904-21960954	HMEC	breast:	n/a
18	chr3:21960904-21960954	HAEpiC	amniotic membrane:	n/a
19	chr3:22192127-22192177	HRCEpiC	kidney:	n/a
20	chr3:22192127-22192177	U87	brain:	n/a
21	chr3:21960904-21960954	NHBE	bronchial:	n/a
22	chr3:22192127-22192177	SK-N-SH	brain:	n/a
23	chr3:22030381-22030431	GM12891	blood:	n/a
24	chr3:21960904-21960954	Jurkat	blood:	n/a
25	chr3:22192127-22192177	Caco-2	colon:	n/a
26	chr3:22030381-22030431	A549	lung:	n/a
27	chr3:21960904-21960954	HCT-116	colon:	n/a
28	chr3:21960904-21960954	HNPCEpiC	eye:	n/a
29	chr3:22192127-22192177	ProgFib	skin:	n/a
30	chr3:22030381-22030431	PANC-1	pancreas:	n/a
31	chr3:22192127-22192177	HRE	kidney:	n/a
32	chr3:22030381-22030431	K562	blood:	n/a
33	chr3:22192127-22192177	SK-N-SH_RA	brain:	n/a
34	chr3:22030381-22030431	HRE	kidney:	n/a
35	chr3:22030381-22030431	U87	brain:	n/a
36	chr3:22030381-22030431	HUVEC	blood vessel:	n/a
37	chr3:22030381-22030431	RPTEC	kidney:	n/a
38	chr3:21960904-21960954	HRCEpiC	kidney:	n/a
39	chr3:22192127-22192177	HRPEpiC	eye:	n/a
40	chr3:22030381-22030431	AG09319	gingival:	n/a
41	chr3:22030381-22030431	LNCaP	prostate:	n/a
42	chr3:21960904-21960954	ECC-1	luminal epithelium:	n/a
43	chr3:22030381-22030431	HCF	heart:	n/a
44	chr3:22192127-22192177	HUVEC	blood vessel:	n/a
45	chr3:22030381-22030431	IMR90	lung:	fetal
46	chr3:21960904-21960954	HRE	kidney:	n/a
47	chr3:22192127-22192177	HEEpiC	esophagus:	n/a
48	chr3:22192127-22192177	HMEC	breast:	n/a
49	chr3:22030381-22030431	HCT-116	colon:	n/a
50	chr3:22030381-22030431	HAEpiC	amniotic membrane:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:22282412..22284259-chr3:22284738..22287975,3	MCF-7	breast:
2	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:
3	chr3:22115704..22118143-chr3:22137096..22138813,2	MCF-7	breast:
4	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
5	chr11:126141332..126144254-chr3:22001697..22003217,2	K562	blood:
6	chr3:22127371..22129495-chr3:22135710..22137615,2	K562	blood:
7	chr3:22217113..22218017-chr3:22727091..22727719,2	MCF-7	breast:
8	chr3:22269821..22272755-chr3:22274788..22276504,2	MCF-7	breast:
9	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
10	chr3:22130623..22131453-chr3:22928892..22930144,3	K562	blood:
11	chr3:21939959..21942443-chr3:21956783..21959351,2	K562	blood:
12	chr3:22195364..22197977-chr3:22208185..22210526,2	K562	blood:
13	chr3:22090916..22093719-chr3:22096309..22098471,5	MCF-7	breast:
14	chr3:22282412..22284259-chr3:22284738..22287975,3	MCF-7	breast:
15	chr3:22060147..22061903-chr3:22064159..22066026,2	K562	blood:
16	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
17	chr3:22269821..22272755-chr3:22274788..22276504,2	MCF-7	breast:
18	chr3:22218049..22218903-chr9:120895826..120896702,2	MCF-7	breast:
19	chr3:22090916..22093719-chr3:22096309..22098471,5	MCF-7	breast:
20	chr3:22042480..22044020-chr3:22057123..22059814,2	K562	blood:
21	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
22	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
23	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
24	chr3:22115704..22118143-chr3:22137096..22138813,2	MCF-7	breast:
25	chr3:22127371..22129495-chr3:22135710..22137615,2	K562	blood:
26	chr3:22042480..22044020-chr3:22057123..22059814,2	K562	blood:
27	chr3:22060147..22061903-chr3:22064159..22066026,2	K562	blood:
28	chr3:22056493..22058211-chr3:22060114..22061974,2	K562	blood:
29	chr3:22051906..22054873-chr3:22056499..22059265,2	K562	blood:
30	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
31	chr3:22056493..22058211-chr3:22060114..22061974,2	K562	blood:
32	chr3:22051906..22054873-chr3:22056499..22059265,2	K562	blood:
33	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
34	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E2-2	chr3:22002908-22003032	ENSG00000223351
2	lnc-UBE2E2-7	chr3:21982020-21982219	l_2330_chr3:21975326-21982219_testes
3	lnc-SGOL1-3	chr3:22175811-22175883	NONHSAT088653
4	lnc-SGOL1-3	chr3:22210309-22210508	NONHSAT088653
5	lnc-UBE2E2-2	chr3:22019707-22019783	ENSG00000223351
6	lnc-UBE2E2-2	chr3:21998631-21998684	ENSG00000223351
7	lnc-SGOL1-3	chr3:22210309-22210443	NONHSAT088650
8	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
9	lnc-UBE2E2-2	chr3:21984058-21984156	ENSG00000223351
10	lnc-SGOL1-3	chr3:22175074-22175484	NONHSAT088653
11	lnc-UBE2E2-7	chr3:21975327-21975419	l_2330_chr3:21975326-21982219_testes
12	lnc-UBE2E2-2	chr3:21998628-21998684	ENSG00000223351
13	lnc-UBE2E2-2	chr3:22021123-22021320	ENSG00000223351
14	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351

No data

Variant related genes	Relation type
ZNF385D-AS2	TF binding region
ZNF385D	TF binding region
ZNF385D-AS2	CpG island
ZNF385D	CpG island
ENSG00000110074	chromatin interactions
ENSG00000151789	chromatin interactions

Extended variants
information (count: 10443 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10443 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10510520	chr3:21955784-21955785	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563657193	chr3:21955800-21955801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553631410	chr3:21955806-21955807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531056446	chr3:21955837-21955838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552355418	chr3:21955861-21955862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs61418462	chr3:21955874-21955875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75556394	chr3:21955886-21955887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs779031	chr3:21955904-21955905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142300149	chr3:21955940-21955941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73129364	chr3:21955947-21955948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs545732350	chr3:21955980-21955981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569507879	chr3:21956019-21956020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565630963	chr3:21956027-21956028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58278871	chr3:21956036-21956037	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs554769212	chr3:21956055-21956056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576120333	chr3:21956096-21956097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139681129	chr3:21956105-21956106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558636300	chr3:21956120-21956121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71310294	chr3:21956132-21956133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576960207	chr3:21956199-21956200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541018432	chr3:21956228-21956229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144436252	chr3:21956242-21956243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181717333	chr3:21956263-21956264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75871008	chr3:21956295-21956296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563922927	chr3:21956345-21956346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538135733	chr3:21956348-21956349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549179907	chr3:21956351-21956352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185848973	chr3:21956353-21956354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558476237	chr3:21956358-21956359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189308642	chr3:21956404-21956405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200010454	chr3:21956417-21956418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528509098	chr3:21956444-21956445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546576267	chr3:21956462-21956463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565864195	chr3:21956471-21956472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530015403	chr3:21956476-21956477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs180901313	chr3:21956479-21956480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376217304	chr3:21956492-21956493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185213721	chr3:21956509-21956510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535244097	chr3:21956514-21956515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569833097	chr3:21956529-21956530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554732912	chr3:21956530-21956531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190313571	chr3:21956532-21956533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558726224	chr3:21956537-21956538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201103163	chr3:21956561-21956562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs397784129	chr3:21956571-21956572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs779030	chr3:21956627-21956628	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543365649	chr3:21956646-21956647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553024252	chr3:21956650-21956651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574318556	chr3:21956659-21956660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141082734	chr3:21956668-21956669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21953800-21956800	Enhancers	Fetal Lung	lung
2	chr3:21954000-21955800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:21954000-21956600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr3:21954000-21956600	Enhancers	NHDF-Ad	bronchial
5	chr3:21954400-21960800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr3:21954600-21955800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:21954600-21956200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:21954600-21956400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:21954800-21957000	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr3:21955400-21956400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:21955400-21960600	Weak transcription	NH-A	brain
12	chr3:21955600-21960600	Weak transcription	Fetal Stomach	stomach
13	chr3:21955600-21960800	Weak transcription	NHLF	lung
14	chr3:21955800-21961200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:21956200-21960600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:21956400-21960800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:21956400-21960800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:21956600-21960400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr3:21956600-21960400	Weak transcription	NHDF-Ad	bronchial
20	chr3:21956800-21957400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:21956800-21957400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr3:21956800-21957400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr3:21956800-21960400	Weak transcription	Fetal Lung	lung
24	chr3:21957000-21957400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:21957000-21960400	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr3:21957400-21960600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:21957400-21960800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:21957400-21960800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr3:21957400-21961000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr3:21960400-21961000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr3:21960400-21961800	Enhancers	Fetal Lung	lung
32	chr3:21960400-21962400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr3:21960400-21963000	Enhancers	NHDF-Ad	bronchial
34	chr3:21960600-21961200	Enhancers	Brain Germinal Matrix	brain
35	chr3:21960600-21961400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr3:21960600-21961800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr3:21960600-21961800	Enhancers	Fetal Stomach	stomach
38	chr3:21960600-21962000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:21960600-21962400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:21960600-21962400	Enhancers	NH-A	brain
41	chr3:21960800-21961000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr3:21960800-21961200	Enhancers	H1 Cell Line	embryonic stem cell
43	chr3:21960800-21961200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr3:21960800-21961200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:21960800-21961600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:21960800-21961800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr3:21960800-21962000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:21960800-21962200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr3:21960800-21962200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:21960800-21962400	Enhancers	Fetal Heart	heart

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