Variant report

Variant	nsv914966
Chromosome Location	chr22:30088442-30138548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1084)
CpG islands
(count:1403)
Chromatin interactive
region (count:48)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1084 , 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	chr22:30097434-30097985	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:30112673-30113047	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:30100619-30100836	HepG2	liver:	n/a	n/a
4	ATF3	chr22:30123277-30123446	K562	blood:	n/a	n/a
5	BACH1	chr22:30117117-30117164	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr22:30101958-30102330	GM12878	blood:	n/a	n/a
7	BHLHE40	chr22:30129772-30130101	K562	blood:	n/a	n/a
8	BHLHE40	chr22:30129783-30130011	GM12878	blood:	n/a	n/a
9	BHLHE40	chr22:30128256-30128610	K562	blood:	n/a	n/a
10	BHLHE40	chr22:30122204-30122269	K562	blood:	n/a	n/a
11	BHLHE40	chr22:30123039-30123491	K562	blood:	n/a	chr22:30123301-30123317 chr22:30123298-30123314
12	BHLHE40	chr22:30112938-30112959	K562	blood:	n/a	n/a
13	BRCA1	chr22:30129764-30130130	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr22:30122729-30123043	K562	blood:	n/a	n/a
15	CBX3	chr22:30128277-30128548	K562	blood:	n/a	n/a
16	CCNT2	chr22:30130069-30130217	K562	blood:	n/a	n/a
17	CCNT2	chr22:30122115-30122354	K562	blood:	n/a	n/a
18	CEBPB	chr22:30120332-30120505	A549	lung:	n/a	chr22:30120448-30120459
19	CEBPB	chr22:30120297-30120612	HepG2	liver:	n/a	chr22:30120448-30120459
20	CEBPB	chr22:30129150-30130110	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr22:30123242-30123551	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr22:30123247-30123550	HepG2	liver:	n/a	n/a
23	CEBPB	chr22:30123279-30123521	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr22:30129437-30129695	K562	blood:	n/a	n/a
25	CEBPB	chr22:30112775-30113097	HepG2	liver:	n/a	n/a
26	CEBPB	chr22:30129330-30129738	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr22:30123253-30123563	K562	blood:	n/a	n/a
28	CEBPB	chr22:30123286-30123530	A549	lung:	n/a	n/a
29	CEBPB	chr22:30112810-30112951	HepG2	liver:	n/a	n/a
30	CEBPB	chr22:30120445-30120468	IMR90	lung:	n/a	chr22:30120448-30120459
31	CEBPB	chr22:30120302-30120606	MCF-7	breast:	n/a	chr22:30120448-30120459
32	CEBPB	chr22:30123245-30123541	IMR90	lung:	n/a	n/a
33	CEBPB	chr22:30112795-30113094	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr22:30123189-30123587	MCF-7	breast:	n/a	n/a
35	CEBPB	chr22:30099063-30099290	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr22:30129294-30130046	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr22:30112804-30113093	IMR90	lung:	n/a	n/a
38	CEBPB	chr22:30129409-30129687	K562	blood:	n/a	n/a
39	CEBPB	chr22:30112805-30112998	K562	blood:	n/a	n/a
40	CEBPB	chr22:30106956-30107195	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr22:30120413-30120592	Hela-S3	cervix:	n/a	chr22:30120448-30120459
42	CEBPD	chr22:30129823-30130320	K562	blood:	n/a	n/a
43	CEBPD	chr22:30123286-30123454	HepG2	liver:	n/a	n/a
44	CHD2	chr22:30129375-30130073	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr22:30122854-30123003	K562	blood:	n/a	n/a
46	CHD2	chr22:30112908-30113057	HepG2	liver:	n/a	n/a
47	CHD2	chr22:30106924-30107562	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr22:30102501-30102765	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr22:30098635-30099768	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr22:30123183-30123203	Fibrobl	skin:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30125642-30125692	GM12891	blood:	n/a
2	chr22:30129607-30129657	IMR90	lung:	fetal
3	chr22:30129607-30129657	AoSMC	blood vessel:	n/a
4	chr22:30122327-30122377	LNCaP	prostate:	n/a
5	chr22:30117734-30117784	SAEC	small airway:	n/a
6	chr22:30116319-30116369	SK-N-SH_RA	brain:	n/a
7	chr22:30091734-30091784	GM19239	blood:	n/a
8	chr22:30116037-30116087	GM12892	blood:	n/a
9	chr22:30116489-30116539	IMR90	lung:	fetal
10	chr22:30117159-30117209	Hepatocyte	liver:	n/a
11	chr22:30117159-30117209	GM19239	blood:	n/a
12	chr22:30129607-30129657	RPTEC	kidney:	n/a
13	chr22:30115203-30115253	HEEpiC	esophagus:	n/a
14	chr22:30116037-30116087	PFSK-1	brain:	n/a
15	chr22:30127118-30127168	HMEC	breast:	n/a
16	chr22:30117148-30117198	SK-N-SH	brain:	n/a
17	chr22:30116953-30117003	MCF-7	breast:	n/a
18	chr22:30116953-30117003	U87	brain:	n/a
19	chr22:30107178-30107228	GM19239	blood:	n/a
20	chr22:30116319-30116369	Jurkat	blood:	n/a
21	chr22:30116919-30116969	PrEC	prostate:	n/a
22	chr22:30125353-30125403	GM12878	blood:	n/a
23	chr22:30129607-30129657	A549	lung:	n/a
24	chr22:30116328-30116378	HRPEpiC	eye:	n/a
25	chr22:30125353-30125403	SK-N-MC	brain:	n/a
26	chr22:30116319-30116369	AG09309	skin:	n/a
27	chr22:30117159-30117209	HCPEpiC	choroid plexus:	n/a
28	chr22:30116489-30116539	PFSK-1	brain:	n/a
29	chr22:30125642-30125692	GM19239	blood:	n/a
30	chr22:30116489-30116539	HNPCEpiC	eye:	n/a
31	chr22:30125353-30125403	NHBE	bronchial:	n/a
32	chr22:30125353-30125403	AG04449	skin:	fetal
33	chr22:30125353-30125403	HUVEC	blood vessel:	n/a
34	chr22:30125353-30125403	HRPEpiC	eye:	n/a
35	chr22:30091734-30091784	SK-N-SH	brain:	n/a
36	chr22:30116953-30117003	ECC-1	luminal epithelium:	n/a
37	chr22:30117159-30117209	Jurkat	blood:	n/a
38	chr22:30129607-30129657	HL-60	blood:	n/a
39	chr22:30122327-30122377	NHBE	bronchial:	n/a
40	chr22:30122327-30122377	Caco-2	colon:	n/a
41	chr22:30117734-30117784	HCT-116	colon:	n/a
42	chr22:30127118-30127168	CMK	blood:	n/a
43	chr22:30116489-30116539	HCT-116	colon:	n/a
44	chr22:30129607-30129657	AG04450	lung:	fetal
45	chr22:30119712-30119762	ECC-1	luminal epithelium:	n/a
46	chr22:30116489-30116539	AG10803	skin:	n/a
47	chr22:30117159-30117209	HAEpiC	amniotic membrane:	n/a
48	chr22:30116319-30116369	HL-60	blood:	n/a
49	chr22:30116328-30116378	Jurkat	blood:	n/a
50	chr22:30115154-30115204	AoSMC	blood vessel:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30118032..30120779-chr22:30154984..30156711,2	K562	blood:
2	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
3	chr22:30091841..30093848-chr22:30094919..30097302,3	MCF-7	breast:
4	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
5	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
6	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
7	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
8	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
9	chr22:30127476..30130014-chr22:30183535..30186061,2	MCF-7	breast:
10	chr22:30098350..30101826-chr22:30195223..30196896,3	MCF-7	breast:
11	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
12	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
13	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
14	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
15	chr22:30120187..30123071-chr22:30140004..30142315,2	K562	blood:
16	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
17	chr22:30094321..30096563-chr22:30160914..30162763,2	MCF-7	breast:
18	chr22:30091841..30093848-chr22:30094919..30097302,3	MCF-7	breast:
19	chr22:30086150..30087724-chr22:30089523..30091656,2	K562	blood:
20	chr22:30126165..30128637-chr22:30161660..30163491,2	MCF-7	breast:
21	chr22:30126344..30127866-chr22:30201046..30202629,2	K562	blood:
22	chr22:30091150..30094109-chr22:30098424..30101093,2	K562	blood:
23	chr22:30114234..30116768-chr22:30120016..30122557,3	MCF-7	breast:
24	chr22:30097693..30098380-chr22:30484799..30485447,2	MCF-7	breast:
25	chr22:30130941..30133818-chr22:30144985..30147499,2	MCF-7	breast:
26	chr22:30091889..30092650-chr22:30194897..30195405,2	MCF-7	breast:
27	chr22:30096098..30098972-chr22:30384609..30387065,2	MCF-7	breast:
28	chr22:30133945..30136337-chr22:30161656..30163853,2	MCF-7	breast:
29	chr22:30098089..30098947-chr22:30484640..30485526,4	MCF-7	breast:
30	chr22:30135111..30137455-chr22:30141470..30144208,2	K562	blood:
31	chr22:30097300..30097855-chr22:30400940..30401466,2	K562	blood:
32	chr22:30122754..30125379-chr22:30128810..30131334,3	MCF-7	breast:
33	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
34	chr22:30117740..30119771-chr22:30165612..30167453,2	MCF-7	breast:
35	chr22:30136102..30138464-chr22:30143800..30146252,2	MCF-7	breast:
36	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
37	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
38	chr22:30091150..30094109-chr22:30098424..30101093,2	K562	blood:
39	chr22:30092151..30092731-chr22:30484958..30485506,2	K562	blood:
40	chr22:30079243..30081163-chr22:30089735..30091351,2	K562	blood:
41	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
42	chr22:30128408..30130433-chr22:30161291..30163799,2	MCF-7	breast:
43	chr22:30122754..30125379-chr22:30128810..30131334,3	MCF-7	breast:
44	chr22:30086357..30088684-chr22:30160929..30163029,2	MCF-7	breast:
45	chr22:30124714..30127862-chr22:30128538..30131492,3	K562	blood:
46	chr22:30097244..30097815-chr22:30485015..30485549,2	MCF-7	breast:
47	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
48	chr22:30124714..30127862-chr22:30128538..30131492,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMAT5-1	chr22:30101245-30101418	XLOC_014338
2	lnc-ZMAT5-1	chr22:30115537-30115848	XLOC_014338
3	lnc-ZMAT5-1	chr22:30107809-30107906	XLOC_014338
4	lnc-ZMAT5-1	chr22:30115537-30115756	NONHSAT084729
5	lnc-ZMAT5-1	chr22:30102120-30102223	XLOC_014338
6	lnc-ZMAT5-1	chr22:30115537-30115737	XLOC_014338
7	lnc-ZMAT5-1	chr22:30115558-30115703	XLOC_014338
8	lnc-ZMAT5-1	chr22:30107802-30107984	XLOC_014338
9	lnc-ZMAT5-1	chr22:30114214-30114787	NONHSAT084729

No data

Variant related genes	Relation type
ENSG00000232396	TF binding region
ENSG00000239446	TF binding region
CABP7	TF binding region
ENSG00000232396	CpG island
ENSG00000239446	CpG island
CABP7	CpG island
ENSG00000100319	chromatin interactions
ENSG00000239446	chromatin interactions
ENSG00000184076	chromatin interactions
ENSG00000100325	chromatin interactions
ENSG00000100314	chromatin interactions
ENSG00000232396	chromatin interactions
NHLRC3	miRNA target sites
NID1	miRNA target sites

Extended variants
information (count: 1996 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1009148	chr22:30088442-30088443	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529639787	chr22:30088481-30088482	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551177465	chr22:30088482-30088483	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533216278	chr22:30088512-30088513	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569485909	chr22:30088551-30088552	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs539519630	chr22:30088581-30088582	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372323867	chr22:30088624-30088625	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs552294073	chr22:30088630-30088631	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558235088	chr22:30088670-30088671	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2267152	chr22:30088671-30088672	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs534187995	chr22:30088682-30088683	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs181312142	chr22:30088692-30088693	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs573577650	chr22:30088713-30088714	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs544135530	chr22:30088750-30088751	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs531730223	chr22:30088761-30088762	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs555909481	chr22:30088796-30088797	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs548261767	chr22:30088797-30088798	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs185188596	chr22:30088805-30088806	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs369866683	chr22:30088834-30088835	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs373410480	chr22:30088863-30088864	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs544733630	chr22:30088890-30088891	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs560204636	chr22:30088928-30088929	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs114405294	chr22:30088954-30088955	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs149524596	chr22:30088981-30088982	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs560899610	chr22:30088997-30088998	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs145529165	chr22:30089017-30089018	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568345012	chr22:30089037-30089038	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189946800	chr22:30089043-30089044	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551318295	chr22:30089136-30089137	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144050309	chr22:30089190-30089191	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533580605	chr22:30089217-30089218	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551726270	chr22:30089258-30089259	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566954827	chr22:30089297-30089298	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148655574	chr22:30089309-30089310	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548950505	chr22:30089386-30089387	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77174118	chr22:30089410-30089411	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs57445516	chr22:30089447-30089448	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113596339	chr22:30089464-30089465	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377298644	chr22:30089496-30089497	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34361449	chr22:30089500-30089501	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556044845	chr22:30089503-30089504	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2283864	chr22:30089511-30089512	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs373235793	chr22:30089512-30089513	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538818957	chr22:30089532-30089533	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553710099	chr22:30089579-30089580	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572089532	chr22:30089649-30089650	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542370448	chr22:30089655-30089656	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2158619	chr22:30089669-30089670	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs147792094	chr22:30089670-30089671	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370709096	chr22:30089678-30089679	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30020800-30097000	Weak transcription	Stomach Mucosa	stomach
2	chr22:30050400-30093000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr22:30054000-30094800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr22:30055400-30095200	Strong transcription	Fetal Intestine Small	intestine
5	chr22:30056000-30094800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr22:30060200-30093600	Strong transcription	Fetal Thymus	thymus
7	chr22:30063400-30094600	Strong transcription	Primary T cells from cord blood	blood
8	chr22:30075400-30097400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr22:30076800-30096400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr22:30077800-30096400	Weak transcription	Small Intestine	intestine
11	chr22:30079600-30097000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr22:30079600-30097400	Weak transcription	Hela-S3	cervix
13	chr22:30080000-30097000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr22:30080200-30089600	Weak transcription	Colonic Mucosa	Colon
15	chr22:30080200-30098800	Weak transcription	GM12878-XiMat	blood
16	chr22:30081000-30096400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr22:30081200-30096400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr22:30081400-30089000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr22:30082000-30088800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr22:30083200-30090000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr22:30083400-30089000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr22:30084000-30089400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr22:30084000-30090000	Weak transcription	Aorta	Aorta
24	chr22:30084200-30088800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr22:30084400-30088600	Weak transcription	Left Ventricle	heart
26	chr22:30084400-30089000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr22:30084400-30089000	Weak transcription	HUVEC	blood vessel
28	chr22:30084400-30089600	Weak transcription	HMEC	breast
29	chr22:30084400-30090400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr22:30084600-30088600	Weak transcription	Gastric	stomach
31	chr22:30084600-30089000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr22:30084600-30089800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr22:30085000-30089000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr22:30085200-30088800	Strong transcription	NHEK	skin
35	chr22:30085600-30092000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr22:30085600-30094000	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr22:30085800-30089000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr22:30085800-30089200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr22:30085800-30089200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr22:30085800-30095000	Strong transcription	Dnd41	blood
41	chr22:30085800-30096200	Weak transcription	Fetal Kidney	kidney
42	chr22:30086000-30089800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr22:30086000-30090000	Weak transcription	Fetal Lung	lung
44	chr22:30086000-30090000	Weak transcription	Osteobl	bone
45	chr22:30086000-30091800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr22:30086000-30092600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr22:30086200-30090000	Genic enhancers	Adipose Nuclei	Adipose
48	chr22:30086200-30090800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr22:30086400-30089200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr22:30086400-30091400	Weak transcription	Brain Substantia Nigra	brain

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