Variant report

Variant	nsv1054220
Chromosome Location	chr12:21612158-21692103
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:979)
CpG islands
(count:1650)
Chromatin interactive
region (count:62)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:21654037-21655206	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:21654435-21654519	K562	blood:	n/a	n/a
3	ARID3A	chr12:21620212-21620571	HepG2	liver:	n/a	n/a
4	ATF1	chr12:21654151-21654868	K562	blood:	n/a	n/a
5	ATF2	chr12:21653889-21654957	GM12878	blood:	n/a	n/a
6	ATF2	chr12:21654047-21654628	GM12878	blood:	n/a	n/a
7	ATF3	chr12:21678978-21679210	K562	blood:	n/a	n/a
8	BACH1	chr12:21680547-21680670	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:21674625-21674693	K562	blood:	n/a	n/a
10	BACH1	chr12:21654911-21655295	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr12:21654206-21654893	A549	lung:	n/a	n/a
12	BCL3	chr12:21654042-21654945	A549	lung:	n/a	n/a
13	BCLAF1	chr12:21654012-21654922	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:21655002-21655161	K562	blood:	n/a	n/a
15	BHLHE40	chr12:21654088-21654723	K562	blood:	n/a	n/a
16	BHLHE40	chr12:21662615-21662820	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:21620389-21620495	HepG2	liver:	n/a	n/a
18	BHLHE40	chr12:21653993-21654978	GM12878	blood:	n/a	chr12:21654891-21654907
19	BRCA1	chr12:21654170-21654839	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr12:21654299-21654864	HepG2	liver:	n/a	n/a
21	BRCA1	chr12:21691197-21691512	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr12:21654343-21654791	GM12878	blood:	n/a	n/a
23	CBX3	chr12:21654147-21654902	K562	blood:	n/a	n/a
24	CCNT2	chr12:21674469-21674678	K562	blood:	n/a	n/a
25	CCNT2	chr12:21654430-21655338	K562	blood:	n/a	n/a
26	CEBPB	chr12:21658538-21658822	K562	blood:	n/a	n/a
27	CEBPB	chr12:21654524-21654905	H1-hESC	embryonic stem cell:	n/a	chr12:21654590-21654598
28	CEBPB	chr12:21676115-21676449	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:21620221-21620588	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:21654022-21654960	GM12878	blood:	n/a	chr12:21654590-21654598
31	CEBPB	chr12:21678916-21679400	A549	lung:	n/a	chr12:21679146-21679157
32	CEBPB	chr12:21679071-21679242	K562	blood:	n/a	chr12:21679146-21679157
33	CEBPB	chr12:21678928-21679487	HCT-116	colon:	n/a	chr12:21679146-21679157
34	CEBPB	chr12:21678962-21679321	K562	blood:	n/a	chr12:21679146-21679157
35	CEBPB	chr12:21679058-21679180	HepG2	liver:	n/a	chr12:21679146-21679157
36	CEBPB	chr12:21678974-21679293	ECC-1	luminal epithelium:	n/a	chr12:21679146-21679157
37	CEBPB	chr12:21654087-21654880	Hela-S3	cervix:	n/a	chr12:21654590-21654598
38	CEBPB	chr12:21679036-21679285	K562	blood:	n/a	chr12:21679146-21679157
39	CEBPB	chr12:21678967-21679310	IMR90	lung:	n/a	chr12:21679146-21679157
40	CEBPB	chr12:21654464-21654849	HepG2	liver:	n/a	chr12:21654590-21654598
41	CEBPB	chr12:21658482-21658823	IMR90	lung:	n/a	n/a
42	CEBPB	chr12:21679034-21679406	MCF-7	breast:	n/a	chr12:21679146-21679157
43	CEBPB	chr12:21678984-21679313	H1-hESC	embryonic stem cell:	n/a	chr12:21679146-21679157
44	CEBPB	chr12:21690968-21691639	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr12:21678966-21679339	Hela-S3	cervix:	n/a	chr12:21679146-21679157
46	CEBPB	chr12:21678961-21679327	HepG2	liver:	n/a	chr12:21679146-21679157
47	CEBPB	chr12:21678873-21679461	A549	lung:	n/a	chr12:21679146-21679157
48	CEBPB	chr12:21678952-21679350	A549	lung:	n/a	chr12:21679146-21679157
49	CHD1	chr12:21653885-21655407	GM12878	blood:	n/a	n/a
50	CHD1	chr12:21654827-21655482	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21655265-21655315	PANC-1	pancreas:	n/a
2	chr12:21680669-21680719	GM12878	blood:	n/a
3	chr12:21681006-21681056	ECC-1	luminal epithelium:	n/a
4	chr12:21655265-21655315	PANC-1	pancreas:	n/a
5	chr12:21680669-21680719	GM12878	blood:	n/a
6	chr12:21681006-21681056	ECC-1	luminal epithelium:	n/a
7	chr12:21654197-21654247	HUVEC	blood vessel:	n/a
8	chr12:21680409-21680459	PFSK-1	brain:	n/a
9	chr12:21654441-21654491	PrEC	prostate:	n/a
10	chr12:21654795-21654845	HEK293	kidney:	embryo
11	chr12:21654508-21654558	Caco-2	colon:	n/a
12	chr12:21654664-21654714	H1-hESC	embryonic stem cell:	embryo
13	chr12:21680981-21681031	MCF10A-Er-Src	breast:	n/a
14	chr12:21654664-21654714	SK-N-SH_RA	brain:	n/a
15	chr12:21654197-21654247	Jurkat	blood:	n/a
16	chr12:21670234-21670284	SK-N-SH_RA	brain:	n/a
17	chr12:21654664-21654714	HEEpiC	esophagus:	n/a
18	chr12:21680669-21680719	PrEC	prostate:	n/a
19	chr12:21654546-21654596	U87	brain:	n/a
20	chr12:21654664-21654714	LNCaP	prostate:	n/a
21	chr12:21651324-21651374	HRCEpiC	kidney:	n/a
22	chr12:21681006-21681056	NB4	blood:	n/a
23	chr12:21654197-21654247	HRPEpiC	eye:	n/a
24	chr12:21678044-21678094	GM12878	blood:	n/a
25	chr12:21654441-21654491	PANC-1	pancreas:	n/a
26	chr12:21680981-21681031	RPTEC	kidney:	n/a
27	chr12:21654664-21654714	NT2-D1	testis:	n/a
28	chr12:21680426-21680476	HNPCEpiC	eye:	n/a
29	chr12:21654287-21654337	HCT-116	colon:	n/a
30	chr12:21670234-21670284	GM12878	blood:	n/a
31	chr12:21680848-21680898	K562	blood:	n/a
32	chr12:21654695-21654745	HepG2	liver:	n/a
33	chr12:21680409-21680459	SK-N-MC	brain:	n/a
34	chr12:21654546-21654596	PFSK-1	brain:	n/a
35	chr12:21681006-21681056	HEEpiC	esophagus:	n/a
36	chr12:21654664-21654714	AG10803	skin:	n/a
37	chr12:21654287-21654337	GM12891	blood:	n/a
38	chr12:21654546-21654596	NH-A	brain:	n/a
39	chr12:21678386-21678436	SK-N-MC	brain:	n/a
40	chr12:21680669-21680719	SK-N-SH_RA	brain:	n/a
41	chr12:21654522-21654572	MCF-7	breast:	n/a
42	chr12:21654441-21654491	Jurkat	blood:	n/a
43	chr12:21655265-21655315	NT2-D1	testis:	n/a
44	chr12:21680508-21680558	NB4	blood:	n/a
45	chr12:21678044-21678094	HAEpiC	amniotic membrane:	n/a
46	chr12:21680981-21681031	U87	brain:	n/a
47	chr12:21654745-21654795	AG09319	gingival:	n/a
48	chr12:21681006-21681056	SK-N-SH	brain:	n/a
49	chr12:21680426-21680476	PANC-1	pancreas:	n/a
50	chr12:21654546-21654596	HEEpiC	esophagus:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:21628037..21630683-chr12:21643280..21645619,2	K562	blood:
2	chr12:21654296..21655290-chr9:135819833..135820422,2	Hela-S3	cervix:
3	chr12:21685388..21686219-chr7:120328726..120329601,2	MCF-7	breast:
4	chr12:21654128..21656631-chr12:21667062..21669279,3	MCF-7	breast:
5	chr12:21649205..21650941-chr3:161087939..161090128,2	MCF-7	breast:
6	chr12:21633395..21635663-chr12:21646507..21648345,2	MCF-7	breast:
7	chr1:9188306..9189002-chr12:21654516..21655344,2	Hela-S3	cervix:
8	chr12:21647474..21650323-chr12:21658442..21660780,2	K562	blood:
9	chr12:21659539..21661221-chr12:21663545..21665442,3	K562	blood:
10	chr12:21667585..21669254-chr12:21672387..21674128,2	K562	blood:
11	chr12:21659626..21662190-chr12:21669299..21671528,2	K562	blood:
12	chr12:21650395..21652297-chr12:21809940..21812051,2	K562	blood:
13	chr12:21632020..21637029-chr12:21648453..21652691,4	K562	blood:
14	chr12:21610148..21613025-chr12:21615165..21617606,4	K562	blood:
15	chr12:21635310..21637987-chr12:21651998..21654175,2	K562	blood:
16	chr12:21628982..21633807-chr12:21637504..21641052,4	K562	blood:
17	chr12:21629462..21631734-chr12:21633503..21635261,2	K562	blood:
18	chr12:21666099..21668505-chr12:21668536..21671439,2	K562	blood:
19	chr12:21654617..21655263-chr12:57481242..57482048,2	Hela-S3	cervix:
20	chr12:21629758..21631544-chr12:21651304..21653537,2	MCF-7	breast:
21	chr12:21628982..21633807-chr12:21637504..21641052,4	K562	blood:
22	chr12:21671832..21674785-chr12:21687913..21690095,2	K562	blood:
23	chr12:21659626..21662190-chr12:21669299..21671528,2	K562	blood:
24	chr12:21631339..21633803-chr12:21653800..21655829,2	K562	blood:
25	chr12:21654009..21656768-chr12:21660013..21662532,3	MCF-7	breast:
26	chr12:21647474..21650323-chr12:21658442..21660780,2	K562	blood:
27	chr12:21635310..21637987-chr12:21651998..21654175,2	K562	blood:
28	chr12:21632566..21634357-chr12:21654067..21655748,2	MCF-7	breast:
29	chr12:21690833..21693060-chr12:21694117..21696142,2	K562	blood:
30	chr12:21627258..21630127-chr12:21631085..21633141,2	K562	blood:
31	chr12:21643281..21645039-chr12:21653322..21655878,2	K562	blood:
32	chr12:21667585..21669254-chr12:21672387..21674128,2	K562	blood:
33	chr12:21628037..21630683-chr12:21643280..21645619,2	K562	blood:
34	chr12:21653863..21655490-chr12:22198033..22200548,2	MCF-7	breast:
35	chr12:21629758..21631544-chr12:21651304..21653537,2	MCF-7	breast:
36	chr12:21653898..21654700-chr3:50378179..50378989,2	Hela-S3	cervix:
37	chr12:21627258..21630127-chr12:21631085..21633141,2	K562	blood:
38	chr12:21632280..21634944-chr12:21765213..21766977,2	K562	blood:
39	chr12:21653310..21655607-chr12:21663313..21666443,3	K562	blood:
40	chr12:21642768..21647284-chr12:21648642..21652273,4	K562	blood:
41	chr12:21654957..21656539-chr12:21677945..21680757,2	K562	blood:
42	chr12:21666099..21668505-chr12:21668536..21671439,2	K562	blood:
43	chr12:21633395..21635663-chr12:21646507..21648345,2	MCF-7	breast:
44	chr12:21689895..21691476-chr12:21725540..21727444,2	K562	blood:
45	chr12:21610148..21613025-chr12:21615165..21617606,4	K562	blood:
46	chr12:21629462..21631734-chr12:21633503..21635261,2	K562	blood:
47	chr12:21657807..21659744-chr12:21755887..21758843,2	MCF-7	breast:
48	chr12:21671832..21674785-chr12:21687913..21690095,2	K562	blood:
49	chr12:21632020..21637029-chr12:21648453..21652691,4	K562	blood:
50	chr12:21643657..21647441-chr12:21652777..21655527,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLT1B-2	chr12:21681935-21682018	NONHSAT027254
2	lnc-GOLT1B-2	chr12:21684071-21685457	NONHSAT027254
3	lnc-GOLT1B-2	chr12:21680870-21681085	NONHSAT027254

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GOLT1B	hsa-miR-103a-3p	chr12:21670976-21670999
2	GOLT1B	hsa-miR-16-5p	chr12:21670982-21671000
3	GOLT1B	hsa-miR-155-5p	chr12:21670582-21670603
4	GOLT1B	hsa-miR-16-5p	chr12:21670993-21670999
5	GOLT1B	hsa-let-7d-5p	chr12:21670264-21670285
6	GOLT1B	hsa-miR-155-5p	chr12:21669700-21669724
7	GOLT1B	hsa-let-7d-5p	chr12:21670278-21670285

Variant related genes	Relation type
RECQL	TF binding region
GOLT1B	TF binding region
PYROXD1	TF binding region
C12orf39	TF binding region
RECQL	CpG island
GOLT1B	CpG island
PYROXD1	CpG island
C12orf39	CpG island
ENSG00000145860	chromatin interactions
ENSG00000186615	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000111711	chromatin interactions
ENSG00000165699	chromatin interactions
ENSG00000111713	chromatin interactions
ENSG00000121350	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000004700	chromatin interactions
ENSG00000134548	chromatin interactions
ENSG00000253256	chromatin interactions
ENSG00000068028	chromatin interactions
ENSG00000111716	chromatin interactions
ENSG00000111726	chromatin interactions
ENSG00000235058	chromatin interactions
ENSG00000180758	chromatin interactions

Extended variants
information (count: 3299 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3299 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6487229	chr12:21612183-21612184	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144235567	chr12:21612242-21612243	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs201922966	chr12:21612246-21612247	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374069002	chr12:21612256-21612257	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs558020244	chr12:21612267-21612268	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs6487230	chr12:21612337-21612338	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs118029062	chr12:21612359-21612360	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs6487231	chr12:21612363-21612364	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs151050260	chr12:21612417-21612418	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs542681712	chr12:21612419-21612420	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs11046067	chr12:21612432-21612433	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35632799	chr12:21612461-21612462	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551460531	chr12:21612486-21612487	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376169309	chr12:21612559-21612560	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs575822402	chr12:21612578-21612579	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs75752500	chr12:21612601-21612602	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs550438112	chr12:21612652-21612653	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs140995334	chr12:21612688-21612689	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs529239977	chr12:21612699-21612700	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs7133827	chr12:21612706-21612707	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs566066259	chr12:21612712-21612713	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs191549530	chr12:21612719-21612720	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs150236205	chr12:21612804-21612805	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs11046068	chr12:21612833-21612834	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537672250	chr12:21612853-21612854	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs557675116	chr12:21612862-21612863	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs536043830	chr12:21612876-21612877	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs539938210	chr12:21612888-21612889	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs367668844	chr12:21612891-21612892	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs7134195	chr12:21612914-21612915	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs73067212	chr12:21612930-21612931	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531991353	chr12:21612935-21612936	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs75975580	chr12:21613004-21613005	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565013802	chr12:21613011-21613012	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200349933	chr12:21613015-21613016	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs116848607	chr12:21613033-21613034	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs544043044	chr12:21613038-21613039	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560845275	chr12:21613097-21613098	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs77084832	chr12:21613102-21613103	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs546496771	chr12:21613103-21613104	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs11046069	chr12:21613114-21613115	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs368887602	chr12:21613119-21613120	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs551565135	chr12:21613122-21613123	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566853549	chr12:21613142-21613143	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs11046070	chr12:21613148-21613149	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs76516114	chr12:21613168-21613169	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs67825288	chr12:21613169-21613170	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs398070051	chr12:21613172-21613173	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs557636478	chr12:21613238-21613239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568237054	chr12:21613265-21613266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2755 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21591800-21614600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr12:21591800-21614800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr12:21591800-21621000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr12:21591800-21624200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:21592000-21614200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr12:21592000-21620600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:21592000-21631000	Weak transcription	Psoas Muscle	Psoas
8	chr12:21592800-21631400	Weak transcription	K562	blood
9	chr12:21593400-21617800	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr12:21594000-21617600	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr12:21594800-21613200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:21595600-21626200	Weak transcription	Right Ventricle	heart
13	chr12:21595800-21624400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr12:21595800-21631400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr12:21595800-21632600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr12:21595800-21633200	Weak transcription	Gastric	stomach
17	chr12:21595800-21650000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:21596000-21631600	Weak transcription	Pancreas	Pancrea
19	chr12:21596200-21625000	Weak transcription	NHLF	lung
20	chr12:21597000-21617800	Strong transcription	Primary B cells from peripheral blood	blood
21	chr12:21597400-21636000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr12:21598000-21620000	Weak transcription	A549	lung
23	chr12:21598200-21617800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:21598400-21617800	Strong transcription	Adipose Nuclei	Adipose
25	chr12:21598600-21617600	Strong transcription	Primary B cells from cord blood	blood
26	chr12:21599000-21624400	Weak transcription	Fetal Brain Male	brain
27	chr12:21599000-21629600	Weak transcription	Stomach Mucosa	stomach
28	chr12:21599200-21614400	Weak transcription	HUVEC	blood vessel
29	chr12:21600000-21624400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:21600400-21624400	Weak transcription	Fetal Kidney	kidney
31	chr12:21602600-21617600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr12:21603800-21612600	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr12:21603800-21613200	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:21606000-21612800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr12:21606800-21613200	Strong transcription	Hela-S3	cervix
36	chr12:21607000-21645800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:21607400-21617600	Strong transcription	Placenta	Placenta
38	chr12:21607600-21617600	Strong transcription	Liver	Liver
39	chr12:21608400-21618200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:21608600-21612400	Strong transcription	Duodenum Mucosa	Duodenum
41	chr12:21608600-21613200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:21608800-21612400	Strong transcription	Fetal Brain Female	brain
43	chr12:21608800-21612800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:21609000-21612200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr12:21609000-21612200	Strong transcription	Brain Hippocampus Middle	brain
46	chr12:21609000-21612400	Strong transcription	HSMM	muscle
47	chr12:21609000-21612600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr12:21609000-21612600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:21609000-21612600	Strong transcription	Brain Anterior Caudate	brain
50	chr12:21609000-21612600	Strong transcription	Brain Germinal Matrix	brain

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