Variant report

Variant	nsv817987
Chromosome Location	chr22:30163526-30169436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:606)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30165743-30166239	HepG2	liver:	n/a	n/a
2	ATF1	chr22:30162842-30163539	K562	blood:	n/a	n/a
3	ATF2	chr22:30162781-30163586	GM12878	blood:	n/a	n/a
4	ATF2	chr22:30163169-30163855	GM12878	blood:	n/a	n/a
5	BHLHE40	chr22:30162608-30163559	K562	blood:	n/a	n/a
6	BHLHE40	chr22:30162705-30163875	GM12878	blood:	n/a	n/a
7	BRCA1	chr22:30162511-30163577	GM12878	blood:	n/a	n/a
8	BRCA1	chr22:30163364-30163721	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr22:30162711-30163672	GM12878	blood:	n/a	chr22:30163165-30163176 chr22:30163165-30163178
10	CEBPB	chr22:30167489-30167690	IMR90	lung:	n/a	chr22:30167595-30167606
11	CEBPB	chr22:30163130-30163554	K562	blood:	n/a	chr22:30163165-30163176 chr22:30163165-30163178
12	CEBPB	chr22:30162837-30163566	Hela-S3	cervix:	n/a	chr22:30163165-30163176 chr22:30163165-30163178
13	CEBPB	chr22:30167486-30167651	HepG2	liver:	n/a	chr22:30167595-30167606
14	CHD1	chr22:30162630-30163772	GM12878	blood:	n/a	n/a
15	CHD2	chr22:30162382-30163581	GM12878	blood:	n/a	n/a
16	CHD2	chr22:30162594-30163599	K562	blood:	n/a	n/a
17	CHD2	chr22:30162635-30163742	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr22:30162393-30163635	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr22:30162561-30163619	HepG2	liver:	n/a	n/a
20	CREB1	chr22:30162669-30163615	K562	blood:	n/a	n/a
21	CREB1	chr22:30162507-30163630	GM12878	blood:	n/a	n/a
22	CREB1	chr22:30162771-30163669	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr22:30162120-30163783	HepG2	liver:	n/a	n/a
24	CREB1	chr22:30162671-30163666	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr22:30162720-30163590	A549	lung:	n/a	n/a
26	CTCF	chr22:30168385-30168507	GM13977	blood:	n/a	n/a
27	CTCF	chr22:30168360-30168510	MCF-7	breast:	n/a	n/a
28	CTCF	chr22:30169260-30169410	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr22:30168352-30168510	GM19238	blood:	n/a	n/a
30	CTCF	chr22:30168322-30168519	GM12892	blood:	n/a	n/a
31	CTCF	chr22:30168340-30168490	AG10803	skin:	n/a	n/a
32	CTCF	chr22:30168420-30168570	GM12874	blood:	n/a	n/a
33	CTCF	chr22:30168380-30168530	GM06990	blood:	n/a	n/a
34	CTCF	chr22:30168380-30168530	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr22:30168680-30168830	WI-38	lung:	n/a	n/a
36	CTCF	chr22:30168308-30168545	Gliobla	brain:	n/a	n/a
37	CTCF	chr22:30168283-30168567	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr22:30168328-30168538	LNCaP	prostate:	n/a	n/a
39	CTCF	chr22:30168240-30168390	A549	lung:	n/a	n/a
40	CTCF	chr22:30168385-30168500	GM10248	blood:	n/a	n/a
41	CTCF	chr22:30168360-30168510	GM12878	blood:	n/a	n/a
42	CTCF	chr22:30168327-30168512	MCF-7	breast:	n/a	n/a
43	CTCF	chr22:30168180-30168470	WI-38	lung:	n/a	n/a
44	CTCF	chr22:30168360-30168510	GM12866	blood:	n/a	n/a
45	CTCF	chr22:30168380-30168530	BE2_C	brain:	n/a	n/a
46	CTCF	chr22:30168360-30168510	HCFaa	heart:	n/a	n/a
47	CTCF	chr22:30168352-30168496	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr22:30168300-30168450	GM12871	blood:	n/a	n/a
49	CTCF	chr22:30168301-30168582	K562	blood:	n/a	n/a
50	CTCF	chr22:30168320-30168470	HCM	heart:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30164162-30164212	HCM	heart:	n/a
2	chr22:30164162-30164212	HAEpiC	amniotic membrane:	n/a
3	chr22:30164162-30164212	HRE	kidney:	n/a
4	chr22:30164162-30164212	RPTEC	kidney:	n/a
5	chr22:30164162-30164212	BJ	skin:	n/a
6	chr22:30165841-30165891	BJ	skin:	n/a
7	chr22:30164162-30164212	Hepatocyte	liver:	n/a
8	chr22:30164162-30164212	T-47D	breast:	n/a
9	chr22:30165841-30165891	HRE	kidney:	n/a
10	chr22:30165841-30165891	HNPCEpiC	eye:	n/a
11	chr22:30164162-30164212	SK-N-SH_RA	brain:	n/a
12	chr22:30165841-30165891	Hepatocyte	liver:	n/a
13	chr22:30164162-30164212	SAEC	small airway:	n/a
14	chr22:30165841-30165891	HL-60	blood:	n/a
15	chr22:30164162-30164212	HEK293	kidney:	embryo
16	chr22:30164162-30164212	ECC-1	luminal epithelium:	n/a
17	chr22:30164162-30164212	NT2-D1	testis:	n/a
18	chr22:30164162-30164212	H1-hESC	embryonic stem cell:	embryo
19	chr22:30165841-30165891	HPAEpiC	pulmonary alveolar:	n/a
20	chr22:30164162-30164212	HNPCEpiC	eye:	n/a
21	chr22:30165841-30165891	NT2-D1	testis:	n/a
22	chr22:30165841-30165891	HCM	heart:	n/a
23	chr22:30164162-30164212	HEEpiC	esophagus:	n/a
24	chr22:30165841-30165891	HAEpiC	amniotic membrane:	n/a
25	chr22:30164162-30164212	HRPEpiC	eye:	n/a
26	chr22:30164162-30164212	U87	brain:	n/a
27	chr22:30164162-30164212	K562	blood:	n/a
28	chr22:30165841-30165891	Caco-2	colon:	n/a
29	chr22:30165841-30165891	HEK293	kidney:	embryo
30	chr22:30165841-30165891	Hela-S3	cervix:	n/a
31	chr22:30165841-30165891	HUVEC	blood vessel:	n/a
32	chr22:30164162-30164212	AG10803	skin:	n/a
33	chr22:30165841-30165891	IMR90	lung:	fetal
34	chr22:30164162-30164212	NHBE	bronchial:	n/a
35	chr22:30164162-30164212	PFSK-1	brain:	n/a
36	chr22:30165841-30165891	U87	brain:	n/a
37	chr22:30164162-30164212	GM06990	blood:	n/a
38	chr22:30165841-30165891	HCPEpiC	choroid plexus:	n/a
39	chr22:30164162-30164212	HL-60	blood:	n/a
40	chr22:30164162-30164212	HRCEpiC	kidney:	n/a
41	chr22:30165841-30165891	SK-N-SH	brain:	n/a
42	chr22:30164162-30164212	SK-N-MC	brain:	n/a
43	chr22:30165841-30165891	HCF	heart:	n/a
44	chr22:30164162-30164212	HCT-116	colon:	n/a
45	chr22:30165841-30165891	GM06990	blood:	n/a
46	chr22:30165841-30165891	AG10803	skin:	n/a
47	chr22:30164162-30164212	LNCaP	prostate:	n/a
48	chr22:30165841-30165891	A549	lung:	n/a
49	chr22:30165841-30165891	NHDF-neo	bronchial:	n/a
50	chr22:30165841-30165891	LNCaP	prostate:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30117740..30119771-chr22:30165612..30167453,2	MCF-7	breast:
2	chr22:30165546..30168026-chr22:30174999..30177192,2	MCF-7	breast:
3	chr22:30167923..30168835-chr22:30389466..30390580,4	MCF-7	breast:
4	chr22:30167962..30168965-chr22:30400516..30401572,3	MCF-7	breast:
5	chr22:30161450..30165931-chr22:30167852..30170164,6	K562	blood:
6	chr22:30162371..30164035-chr22:30233277..30234908,2	MCF-7	breast:
7	chr22:30168312..30170013-chr22:30216889..30218868,2	MCF-7	breast:
8	chr22:30168082..30170314-chr22:30185958..30187695,2	MCF-7	breast:
9	chr22:30145045..30147687-chr22:30166151..30168873,2	MCF-7	breast:
10	chr22:30161121..30163790-chr22:30207742..30209725,2	MCF-7	breast:
11	chr22:30167944..30169824-chr22:30191784..30194571,2	MCF-7	breast:
12	chr22:30165843..30167692-chr22:30176073..30180493,3	MCF-7	breast:
13	chr22:30161539..30163655-chr22:30194119..30196895,2	K562	blood:
14	chr17:80186628..80187493-chr22:30163288..30163911,2	HCT-116	colon:
15	chr22:30161269..30163676-chr22:30230353..30231980,2	MCF-7	breast:
16	chr22:30160959..30163738-chr22:30164422..30168687,4	MCF-7	breast:

No data

Variant related genes	Relation type
ZMAT5	TF binding region
ZMAT5	CpG island
ENSG00000100325	chromatin interactions
ENSG00000100319	chromatin interactions
ENSG00000184076	chromatin interactions
ENSG00000141526	chromatin interactions

Extended variants
information (count: 203 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:203 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76013375	chr22:30163526-30163527	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs552806899	chr22:30163534-30163535	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs372992419	chr22:30163542-30163543	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs376290630	chr22:30163554-30163555	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200176748	chr22:30163571-30163572	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs374129740	chr22:30163597-30163598	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs370069820	chr22:30163631-30163632	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs532042151	chr22:30163640-30163641	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs180878075	chr22:30163657-30163658	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534834445	chr22:30163719-30163720	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs140135	chr22:30163835-30163836	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs569965271	chr22:30163919-30163920	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532613223	chr22:30163925-30163926	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554664649	chr22:30163945-30163946	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535363240	chr22:30164064-30164065	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374402521	chr22:30164209-30164210	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs185333042	chr22:30164217-30164218	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs115595018	chr22:30164287-30164288	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs139348486	chr22:30164293-30164294	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs569761080	chr22:30164295-30164296	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs375549411	chr22:30164298-30164299	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs184101675	chr22:30164311-30164312	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs16988025	chr22:30164369-30164370	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs570589614	chr22:30164380-30164381	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs534537269	chr22:30164439-30164440	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs144094912	chr22:30164479-30164480	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs12158466	chr22:30164511-30164512	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs574577222	chr22:30164533-30164534	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs186630137	chr22:30164550-30164551	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs199719762	chr22:30164607-30164608	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs556949282	chr22:30164614-30164615	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs575323739	chr22:30164615-30164616	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs386820603	chr22:30164616-30164617	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs150623347	chr22:30164617-30164618	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532870343	chr22:30164618-30164619	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs12627756	chr22:30164621-30164622	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs368297891	chr22:30164625-30164626	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs386820604	chr22:30164626-30164627	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs140138	chr22:30164628-30164629	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
40	rs199967352	chr22:30164629-30164630	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs530129022	chr22:30164722-30164723	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs139520152	chr22:30164765-30164766	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs563301528	chr22:30164773-30164774	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs377101531	chr22:30164797-30164798	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs552417714	chr22:30164828-30164829	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs570642224	chr22:30164843-30164844	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs534960042	chr22:30164891-30164892	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534472200	chr22:30164896-30164897	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs553851404	chr22:30164902-30164903	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568265591	chr22:30164915-30164916	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30161000-30164000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr22:30161800-30164000	Active TSS	Rectal Smooth Muscle	rectum
3	chr22:30161800-30164200	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr22:30161800-30164800	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr22:30162000-30164000	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr22:30162000-30164200	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr22:30162000-30164400	Active TSS	HSMM	muscle
8	chr22:30162000-30164600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr22:30162000-30164600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr22:30162000-30164600	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr22:30162000-30164600	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr22:30162000-30164600	Active TSS	A549	lung
13	chr22:30162200-30164000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr22:30162200-30164000	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr22:30162200-30164200	Active TSS	Aorta	Aorta
16	chr22:30162200-30164200	Active TSS	Ovary	ovary
17	chr22:30162200-30164200	Active TSS	NHDF-Ad	bronchial
18	chr22:30162400-30163600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr22:30162400-30163800	Active TSS	Brain Substantia Nigra	brain
20	chr22:30162400-30164000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr22:30162400-30164000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr22:30162400-30164000	Active TSS	Primary T helper naive cells from peripheral blood	blood
23	chr22:30162400-30164000	Active TSS	Esophagus	oesophagus
24	chr22:30162400-30164000	Active TSS	Fetal Lung	lung
25	chr22:30162400-30164000	Active TSS	Gastric	stomach
26	chr22:30162400-30164000	Active TSS	Small Intestine	intestine
27	chr22:30162400-30164000	Active TSS	HMEC	breast
28	chr22:30162400-30164000	Active TSS	HSMMtube	muscle
29	chr22:30162400-30164200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr22:30162400-30164200	Active TSS	H1 Cell Line	embryonic stem cell
31	chr22:30162400-30164200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr22:30162400-30164200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr22:30162400-30164200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr22:30162400-30164200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr22:30162400-30164200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr22:30162400-30164200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr22:30162400-30164200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr22:30162400-30164200	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr22:30162400-30164200	Active TSS	Fetal Intestine Large	intestine
40	chr22:30162400-30164200	Active TSS	Fetal Intestine Small	intestine
41	chr22:30162400-30164200	Active TSS	Fetal Kidney	kidney
42	chr22:30162400-30164200	Active TSS	Psoas Muscle	Psoas
43	chr22:30162400-30164200	Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr22:30162400-30164200	Active TSS	GM12878-XiMat	blood
45	chr22:30162400-30164200	Bivalent/Poised TSS	HepG2	liver
46	chr22:30162400-30164400	Active TSS	H9 Cell Line	embryonic stem cell
47	chr22:30162400-30164400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr22:30162400-30164400	Active TSS	K562	blood
49	chr22:30162600-30163600	Active TSS	Primary T cells from cord blood	blood
50	chr22:30162600-30163600	Active TSS	Primary hematopoietic stem cells	blood

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