Variant report

Variant	nsv945912
Chromosome Location	chr1:45243841-45248516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:45244454-45244967	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:45246112-45246941	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:45245241-45245566	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr1:45246376-45247474	A549	lung:	n/a	n/a
5	BCL3	chr1:45246453-45246842	GM12878	blood:	n/a	n/a
6	BCL3	chr1:45248265-45248772	A549	lung:	n/a	n/a
7	BCLAF1	chr1:45246704-45247030	GM12878	blood:	n/a	n/a
8	BCLAF1	chr1:45245616-45246834	K562	blood:	n/a	n/a
9	BCLAF1	chr1:45246167-45247108	GM12878	blood:	n/a	n/a
10	BRCA1	chr1:45246808-45246852	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr1:45246719-45246916	K562	blood:	n/a	n/a
12	CEBPB	chr1:45245703-45246198	K562	blood:	n/a	n/a
13	CEBPD	chr1:45244936-45245531	K562	blood:	n/a	n/a
14	CEBPD	chr1:45245806-45246562	K562	blood:	n/a	n/a
15	CHD2	chr1:45246192-45247184	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:45246631-45246680	HepG2	liver:	n/a	n/a
17	CTCF	chr1:45244182-45244405	T-47D	breast:	n/a	n/a
18	CTCF	chr1:45246620-45246770	K562	blood:	n/a	n/a
19	CTCF	chr1:45246564-45246697	HepG2	liver:	n/a	n/a
20	CTCF	chr1:45246640-45246790	Caco-2	colon:	n/a	n/a
21	CTCF	chr1:45246520-45246670	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr1:45246610-45246697	K562	blood:	n/a	n/a
23	CTCF	chr1:45246600-45246750	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr1:45246560-45246710	HEK293	kidney:	n/a	n/a
25	EBF1	chr1:45244421-45244751	GM12878	blood:	n/a	n/a
26	EP300	chr1:45244162-45244505	T-47D	breast:	n/a	n/a
27	FOSL2	chr1:45245979-45246648	HepG2	liver:	n/a	n/a
28	HEY1	chr1:45245231-45247342	HepG2	liver:	n/a	n/a
29	HEY1	chr1:45245623-45246882	K562	blood:	n/a	n/a
30	HEY1	chr1:45245252-45245557	K562	blood:	n/a	n/a
31	HEY1	chr1:45244410-45245079	HepG2	liver:	n/a	n/a
32	HEY1	chr1:45243835-45245001	HepG2	liver:	n/a	n/a
33	HEY1	chr1:45245245-45245539	HepG2	liver:	n/a	n/a
34	HEY1	chr1:45243695-45244848	K562	blood:	n/a	n/a
35	HEY1	chr1:45245582-45247381	HepG2	liver:	n/a	n/a
36	HEY1	chr1:45240457-45247308	K562	blood:	n/a	n/a
37	HEY1	chr1:45243859-45244323	HepG2	liver:	n/a	n/a
38	JUND	chr1:45246415-45246539	H1-hESC	embryonic stem cell:	n/a	n/a
39	JUND	chr1:45246204-45246368	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr1:45246390-45246912	A549	lung:	n/a	n/a
41	JUND	chr1:45244050-45244077	H1-hESC	embryonic stem cell:	n/a	n/a
42	KAP1	chr1:45244852-45244885	U2OS	brain:	n/a	n/a
43	MAZ	chr1:45246599-45246661	K562	blood:	n/a	n/a
44	MTA3	chr1:45244377-45244869	GM12878	blood:	n/a	n/a
45	MTA3	chr1:45245655-45247618	GM12878	blood:	n/a	n/a
46	MTA3	chr1:45246139-45246569	GM12878	blood:	n/a	n/a
47	MTA3	chr1:45246585-45247476	GM12878	blood:	n/a	n/a
48	MTA3	chr1:45247655-45248170	GM12878	blood:	n/a	n/a
49	MYC	chr1:45246293-45246438	MCF-7	breast:	n/a	n/a
50	MYC	chr1:45246351-45246435	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45243960-45244010	AG04450	lung:	fetal
2	chr1:45243960-45244010	HRE	kidney:	n/a
3	chr1:45246038-45246088	GM19239	blood:	n/a
4	chr1:45243960-45244010	HNPCEpiC	eye:	n/a
5	chr1:45246038-45246088	AG04450	lung:	fetal
6	chr1:45246038-45246088	BJ	skin:	n/a
7	chr1:45243960-45244010	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:45243960-45244010	ovcar-3	ovarian:	n/a
9	chr1:45246038-45246088	HUVEC	blood vessel:	n/a
10	chr1:45244184-45244234	T-47D	breast:	n/a
11	chr1:45246038-45246088	U87	brain:	n/a
12	chr1:45246038-45246088	Jurkat	blood:	n/a
13	chr1:45246038-45246088	ovcar-3	ovarian:	n/a
14	chr1:45246038-45246088	ProgFib	skin:	n/a
15	chr1:45244184-45244234	Jurkat	blood:	n/a
16	chr1:45243960-45244010	Hepatocyte	liver:	n/a
17	chr1:45246038-45246088	Hela-S3	cervix:	n/a
18	chr1:45243960-45244010	CMK	blood:	n/a
19	chr1:45243960-45244010	HRCEpiC	kidney:	n/a
20	chr1:45246038-45246088	SK-N-MC	brain:	n/a
21	chr1:45244184-45244234	HCF	heart:	n/a
22	chr1:45244184-45244234	HCM	heart:	n/a
23	chr1:45243960-45244010	H1-hESC	embryonic stem cell:	embryo
24	chr1:45246038-45246088	HRPEpiC	eye:	n/a
25	chr1:45243960-45244010	PrEC	prostate:	n/a
26	chr1:45243960-45244010	MCF10A-Er-Src	breast:	n/a
27	chr1:45244184-45244234	MCF-7	breast:	n/a
28	chr1:45244184-45244234	AG09319	gingival:	n/a
29	chr1:45243960-45244010	HEK293	kidney:	embryo
30	chr1:45243960-45244010	GM06990	blood:	n/a
31	chr1:45246038-45246088	HepG2	liver:	n/a
32	chr1:45244184-45244234	IMR90	lung:	fetal
33	chr1:45243960-45244010	HMEC	breast:	n/a
34	chr1:45244184-45244234	AG04449	skin:	fetal
35	chr1:45243960-45244010	HCM	heart:	n/a
36	chr1:45244184-45244234	NT2-D1	testis:	n/a
37	chr1:45246038-45246088	NHDF-neo	bronchial:	n/a
38	chr1:45244184-45244234	ProgFib	skin:	n/a
39	chr1:45246038-45246088	ECC-1	luminal epithelium:	n/a
40	chr1:45243960-45244010	U87	brain:	n/a
41	chr1:45244184-45244234	PrEC	prostate:	n/a
42	chr1:45246038-45246088	A549	lung:	n/a
43	chr1:45246038-45246088	HCPEpiC	choroid plexus:	n/a
44	chr1:45244184-45244234	NH-A	brain:	n/a
45	chr1:45243960-45244010	NT2-D1	testis:	n/a
46	chr1:45243960-45244010	RPTEC	kidney:	n/a
47	chr1:45246038-45246088	T-47D	breast:	n/a
48	chr1:45244184-45244234	CMK	blood:	n/a
49	chr1:45246038-45246088	GM12891	blood:	n/a
50	chr1:45246038-45246088	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:45239942..45244585-chr1:45273690..45277023,5	MCF-7	breast:
2	chr1:45239592..45244618-chr1:45476667..45480609,10	K562	blood:
3	chr1:45239135..45244789-chr1:45475459..45482236,15	K562	blood:
4	chr1:45246917..45250948-chr1:45965225..45967473,3	K562	blood:
5	chr1:45246681..45259677-chr1:45281336..45290057,25	MCF-7	breast:
6	chr1:45194515..45198714-chr1:45239955..45244261,13	MCF-7	breast:
7	chr1:45248466..45253060-chr1:45282997..45288611,7	MCF-7	breast:
8	chr1:45248330..45252127-chr1:45262500..45268022,8	MCF-7	breast:
9	chr1:45239101..45240995-chr1:45242933..45244701,2	MCF-7	breast:
10	chr1:45193566..45196499-chr1:45246618..45248474,2	MCF-7	breast:
11	chr1:45238319..45262026-chr1:45262351..45301953,358	K562	blood:
12	chr1:45239959..45246724-chr1:45282430..45287057,13	MCF-7	breast:
13	chr1:45245131..45247941-chr1:45805894..45808200,2	K562	blood:
14	chr1:45246411..45248469-chr1:45275602..45279033,3	MCF-7	breast:
15	chr1:45248400..45253844-chr1:45268438..45273783,8	MCF-7	breast:
16	chr1:45194298..45199848-chr1:45247467..45253056,11	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000225721	TF binding region
RPS15AP11	TF binding region
SNORD38B	TF binding region
ENSG00000225721	CpG island
RPS15AP11	CpG island
SNORD38B	CpG island
ENSG00000200169	chromatin interactions
ENSG00000132763	chromatin interactions
ENSG00000142937	chromatin interactions
ENSG00000173846	chromatin interactions
ENSG00000126088	chromatin interactions
ENSG00000188396	chromatin interactions
ENSG00000126107	chromatin interactions
ENSG00000117425	chromatin interactions
ENSG00000132773	chromatin interactions
ENSG00000132781	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000222009	chromatin interactions
ENSG00000236624	chromatin interactions

Extended variants
information (count: 211 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:211 , 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	rs76452876	chr1:45243853-45243854	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs150427317	chr1:45243858-45243859	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs552300925	chr1:45243875-45243876	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs535541551	chr1:45243917-45243918	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs555528457	chr1:45243927-45243928	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs74073404	chr1:45243957-45243958	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs186425812	chr1:45243977-45243978	Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs557343915	chr1:45244010-45244011	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs201847423	chr1:45244013-45244014	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs142345455	chr1:45244025-45244026	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs34433949	chr1:45244030-45244031	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs546043601	chr1:45244048-45244049	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs3838955	chr1:45244051-45244052	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs397703859	chr1:45244052-45244053	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs371153216	chr1:45244072-45244073	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs374217599	chr1:45244094-45244095	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs553145469	chr1:45244110-45244111	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs573149902	chr1:45244153-45244154	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs376189539	chr1:45244178-45244179	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs561860661	chr1:45244185-45244186	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs374943975	chr1:45244217-45244218	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs139479202	chr1:45244233-45244234	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs374827889	chr1:45244239-45244240	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs112465738	chr1:45244246-45244247	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs201044480	chr1:45244255-45244256	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs11537871	chr1:45244267-45244268	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs1061669	chr1:45244310-45244311	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs1061674	chr1:45244325-45244326	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs115900939	chr1:45244330-45244331	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs11411	chr1:45244338-45244339	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs190973585	chr1:45244347-45244348	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs200072783	chr1:45244376-45244377	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs372406082	chr1:45244377-45244378	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs113628443	chr1:45244411-45244412	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs34091414	chr1:45244454-45244455	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs182266530	chr1:45244477-45244478	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs549066303	chr1:45244511-45244512	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs568956250	chr1:45244512-45244513	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs146302789	chr1:45244540-45244541	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs551366465	chr1:45244582-45244583	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs149685894	chr1:45244592-45244593	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs539744536	chr1:45244608-45244609	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs76421881	chr1:45244620-45244621	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs10465818	chr1:45244692-45244693	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs535672487	chr1:45244699-45244700	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs555529602	chr1:45244726-45244727	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs148865116	chr1:45244759-45244760	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs191054260	chr1:45244769-45244770	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs183289941	chr1:45244788-45244789	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs143287984	chr1:45244802-45244803	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45240600-45244000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:45241600-45244200	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
3	chr1:45241600-45244200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:45241600-45244200	Transcr. at gene 5' and 3'	NHEK	skin
5	chr1:45241600-45244600	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
6	chr1:45241600-45244600	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
7	chr1:45241600-45244600	Transcr. at gene 5' and 3'	Dnd41	blood
8	chr1:45241600-45244800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:45241800-45244000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
10	chr1:45241800-45244200	Transcr. at gene 5' and 3'	NHLF	lung
11	chr1:45241800-45244800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:45241800-45244800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:45241800-45244800	Transcr. at gene 5' and 3'	A549	lung
14	chr1:45241800-45244800	Transcr. at gene 5' and 3'	K562	blood
15	chr1:45241800-45245000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
16	chr1:45242000-45244000	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
17	chr1:45242000-45244000	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:45242000-45244200	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:45242000-45244400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
20	chr1:45242000-45244600	Transcr. at gene 5' and 3'	HepG2	liver
21	chr1:45242000-45245000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:45242000-45245000	Transcr. at gene 5' and 3'	Hela-S3	cervix
23	chr1:45242200-45244000	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:45242200-45244000	Transcr. at gene 5' and 3'	HMEC	breast
25	chr1:45242200-45244400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
26	chr1:45242200-45244600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:45242200-45244600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:45242200-45244800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
29	chr1:45242400-45244000	Transcr. at gene 5' and 3'	HUVEC	blood vessel
30	chr1:45242400-45244600	Transcr. at gene 5' and 3'	NH-A	brain
31	chr1:45242400-45244800	Genic enhancers	Stomach Mucosa	stomach
32	chr1:45242400-45246400	Strong transcription	Aorta	Aorta
33	chr1:45242600-45244200	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr1:45242600-45244200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
35	chr1:45242600-45244200	Enhancers	Fetal Brain Male	brain
36	chr1:45242600-45244200	Genic enhancers	Pancreas	Pancrea
37	chr1:45242600-45244200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
38	chr1:45242600-45244200	Genic enhancers	Thymus	Thymus
39	chr1:45242600-45244200	Genic enhancers	Monocytes-CD14+_RO01746	blood
40	chr1:45242600-45244600	Genic enhancers	Primary B cells from peripheral blood	blood
41	chr1:45242600-45244600	Genic enhancers	Placenta	Placenta
42	chr1:45242600-45247600	Strong transcription	Brain Hippocampus Middle	brain
43	chr1:45242800-45244000	Genic enhancers	Colonic Mucosa	Colon
44	chr1:45242800-45244000	Genic enhancers	Fetal Lung	lung
45	chr1:45242800-45244000	Genic enhancers	Left Ventricle	heart
46	chr1:45242800-45244200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:45242800-45244200	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:45242800-45244200	Genic enhancers	Adipose Nuclei	Adipose
49	chr1:45242800-45244600	Genic enhancers	Fetal Muscle Trunk	muscle
50	chr1:45242800-45244600	Strong transcription	Small Intestine	intestine

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