Variant report

Variant	esv2751056
Chromosome Location	chr12:31239600-31406809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2082)
CpG islands
(count:1465)
Chromatin interactive
region (count:28)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2082 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31391820-31391981	K562	blood:	n/a	n/a
2	ARID3A	chr12:31399086-31399282	HepG2	liver:	n/a	n/a
3	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
4	ATF1	chr12:31365662-31365782	K562	blood:	n/a	n/a
5	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
7	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
9	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
13	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
14	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
15	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
16	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
17	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
19	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:31390019-31390036	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
26	BRCA1	chr12:31391842-31392078	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr12:31358885-31359398	HCT-116	colon:	n/a	n/a
28	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
29	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
30	CEBPB	chr12:31355347-31355432	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
32	CEBPB	chr12:31391866-31392108	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
34	CEBPB	chr12:31391806-31392080	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:31395234-31395493	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
37	CEBPB	chr12:31395273-31395514	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:31401830-31402026	HepG2	liver:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
40	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
41	CEBPB	chr12:31401823-31402021	Hela-S3	cervix:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
42	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
43	CHD2	chr12:31371770-31371778	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr12:31358885-31359207	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr12:31270114-31270314	GM12878	blood:	n/a	n/a
46	CHD2	chr12:31271857-31272216	K562	blood:	n/a	n/a
47	CHD2	chr12:31270194-31270459	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr12:31271851-31272155	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr12:31271974-31272145	GM12878	blood:	n/a	n/a
50	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31405499-31405549	PrEC	prostate:	n/a
2	chr12:31405499-31405549	PrEC	prostate:	n/a
3	chr12:31402470-31402520	HRCEpiC	kidney:	n/a
4	chr12:31360362-31360412	SK-N-SH_RA	brain:	n/a
5	chr12:31257362-31257412	BJ	skin:	n/a
6	chr12:31405369-31405419	NB4	blood:	n/a
7	chr12:31255279-31255329	MCF10A-Er-Src	breast:	n/a
8	chr12:31255279-31255329	AG04450	lung:	fetal
9	chr12:31405499-31405549	Jurkat	blood:	n/a
10	chr12:31402470-31402520	AG10803	skin:	n/a
11	chr12:31254036-31254086	GM06990	blood:	n/a
12	chr12:31241496-31241546	HIPEpiC	eye:	n/a
13	chr12:31405499-31405549	RPTEC	kidney:	n/a
14	chr12:31272112-31272162	GM12878	blood:	n/a
15	chr12:31370930-31370980	K562	blood:	n/a
16	chr12:31272112-31272162	HL-60	blood:	n/a
17	chr12:31360362-31360412	AG09309	skin:	n/a
18	chr12:31271429-31271479	AG04449	skin:	fetal
19	chr12:31272112-31272162	ovcar-3	ovarian:	n/a
20	chr12:31402470-31402520	Caco-2	colon:	n/a
21	chr12:31402470-31402520	Jurkat	blood:	n/a
22	chr12:31271783-31271833	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:31276852-31276902	HCF	heart:	n/a
24	chr12:31272865-31272915	RPTEC	kidney:	n/a
25	chr12:31316348-31316398	NHDF-neo	bronchial:	n/a
26	chr12:31405499-31405549	BJ	skin:	n/a
27	chr12:31257362-31257412	PANC-1	pancreas:	n/a
28	chr12:31256838-31256888	A549	lung:	n/a
29	chr12:31405359-31405409	HCT-116	colon:	n/a
30	chr12:31274424-31274474	BE2_C	brain:	n/a
31	chr12:31405359-31405409	PrEC	prostate:	n/a
32	chr12:31272119-31272169	BJ	skin:	n/a
33	chr12:31406441-31406491	AG09319	gingival:	n/a
34	chr12:31370930-31370980	T-47D	breast:	n/a
35	chr12:31378024-31378074	BE2_C	brain:	n/a
36	chr12:31271429-31271479	AG09309	skin:	n/a
37	chr12:31405359-31405409	Hela-S3	cervix:	n/a
38	chr12:31270326-31270376	NB4	blood:	n/a
39	chr12:31272119-31272169	ECC-1	luminal epithelium:	n/a
40	chr12:31402470-31402520	LNCaP	prostate:	n/a
41	chr12:31256838-31256888	GM12892	blood:	n/a
42	chr12:31272119-31272169	HCF	heart:	n/a
43	chr12:31274424-31274474	NB4	blood:	n/a
44	chr12:31254007-31254057	PrEC	prostate:	n/a
45	chr12:31274424-31274474	T-47D	breast:	n/a
46	chr12:31274424-31274474	SK-N-SH	brain:	n/a
47	chr12:31271783-31271833	ECC-1	luminal epithelium:	n/a
48	chr12:31241496-31241546	T-47D	breast:	n/a
49	chr12:31406441-31406491	SKMC	muscle:	n/a
50	chr12:31370930-31370980	Caco-2	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
2	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
3	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
4	chr12:31269317..31270662-chr12:31391620..31392355,3	MCF-7	breast:
5	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
6	chr12:31388279..31391169-chr12:31396495..31398764,2	K562	blood:
7	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
8	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
9	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
10	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
11	chr12:31269781..31270824-chr12:31398705..31400061,4	MCF-7	breast:
12	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
13	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
14	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
15	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
16	chr12:31269943..31270748-chr12:31391487..31392373,2	K562	blood:
17	chr12:31391273..31391961-chr12:31404788..31405659,2	K562	blood:
18	chr12:31358059..31360304-chr12:31368898..31371452,2	MCF-7	breast:
19	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
20	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
21	chr12:30999874..31000492-chr12:31398859..31399728,2	K562	blood:
22	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
23	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
24	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
25	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
26	chr12:31354080..31355986-chr12:31357943..31360954,3	K562	blood:
27	chr12:31399111..31400912-chr12:31476871..31479529,2	MCF-7	breast:
28	chr12:31354464..31355986-chr12:31358238..31360954,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-4	chr12:31367135-31367371	expReg_chr12_2391_-
2	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
3	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
4	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
5	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
6	lnc-AC024940.1-3	chr12:31397374-31397619	NONHSAT027541
7	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066

No data

Variant related genes	Relation type
ENSG00000270926	TF binding region
ENSG00000270766	TF binding region
ENSG00000243517	TF binding region
ENSG00000177359	TF binding region
DDX11	TF binding region
ENSG00000270926	CpG island
ENSG00000270766	CpG island
ENSG00000243517	CpG island
ENSG00000177359	CpG island
DDX11	CpG island
ENSG00000270766	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000177340	chromatin interactions

Extended variants
information (count: 4826 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4826 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2352624	chr12:31239600-31239601	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570520549	chr12:31239630-31239631	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs2260149	chr12:31239637-31239638	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534664973	chr12:31239640-31239641	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs61119439	chr12:31239659-31239660	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs566994868	chr12:31239680-31239681	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189806214	chr12:31239694-31239695	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs180894759	chr12:31239699-31239700	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs2553133	chr12:31239704-31239705	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
10	rs7304510	chr12:31239796-31239797	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545919684	chr12:31239860-31239861	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs564131619	chr12:31239872-31239873	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201532675	chr12:31239908-31239909	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs142783476	chr12:31239910-31239911	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs560027129	chr12:31239931-31239932	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs530316644	chr12:31239948-31239949	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs116577228	chr12:31239966-31239967	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs2536772	chr12:31239973-31239974	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs185893569	chr12:31239984-31239985	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531092802	chr12:31240075-31240076	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs552267772	chr12:31240082-31240083	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs573977559	chr12:31240098-31240099	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs61917217	chr12:31240099-31240100	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs71452271	chr12:31240125-31240126	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2909385	chr12:31240126-31240127	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs2911830	chr12:31240133-31240134	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2909386	chr12:31240145-31240146	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557174485	chr12:31240169-31240170	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs575360339	chr12:31240256-31240257	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs545989209	chr12:31240325-31240326	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs577816005	chr12:31240328-31240329	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs10743750	chr12:31240334-31240335	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs572956321	chr12:31240418-31240419	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192030957	chr12:31240432-31240433	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs7308368	chr12:31240502-31240503	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs28420982	chr12:31240514-31240515	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
37	rs542167790	chr12:31240515-31240516	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs563971399	chr12:31240566-31240567	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs531031131	chr12:31240606-31240607	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs376224303	chr12:31240608-31240609	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs564274972	chr12:31240609-31240610	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs35384711	chr12:31240611-31240612	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs7308492	chr12:31240617-31240618	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs7308494	chr12:31240622-31240623	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs2543270	chr12:31240635-31240636	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535802610	chr12:31240673-31240674	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs61917218	chr12:31240694-31240695	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs182033912	chr12:31240717-31240718	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs569109149	chr12:31240735-31240736	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs61917219	chr12:31240736-31240737	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	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
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227800-31240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr12:31227800-31242000	Weak transcription	Left Ventricle	heart
3	chr12:31227800-31242600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
5	chr12:31228000-31242000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr12:31228000-31244400	Weak transcription	Fetal Kidney	kidney
7	chr12:31228000-31244600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:31228000-31249200	Weak transcription	Brain Angular Gyrus	brain
9	chr12:31228000-31255000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr12:31228000-31256400	Weak transcription	Liver	Liver
11	chr12:31228000-31258200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:31228000-31269800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:31228200-31261800	Weak transcription	Brain Substantia Nigra	brain
14	chr12:31228400-31240400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr12:31228400-31259800	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr12:31229000-31256200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:31229400-31241000	Weak transcription	GM12878-XiMat	blood
18	chr12:31230800-31258000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr12:31231800-31242000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr12:31232000-31251800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:31232200-31249400	Weak transcription	Osteobl	bone
22	chr12:31232400-31247800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:31232800-31251000	Strong transcription	Duodenum Mucosa	Duodenum
24	chr12:31233400-31250400	Strong transcription	Dnd41	blood
25	chr12:31233400-31257400	Weak transcription	NHEK	skin
26	chr12:31233400-31259000	Weak transcription	NH-A	brain
27	chr12:31233400-31259800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:31233800-31247000	Weak transcription	HSMM	muscle
29	chr12:31233800-31256400	Weak transcription	HUVEC	blood vessel
30	chr12:31233800-31256600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:31233800-31260800	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr12:31234000-31242800	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr12:31234000-31251200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr12:31234000-31252200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:31234000-31257600	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr12:31234200-31242800	Strong transcription	Fetal Muscle Leg	muscle
37	chr12:31234400-31256400	Weak transcription	HMEC	breast
38	chr12:31234400-31256600	Weak transcription	Hela-S3	cervix
39	chr12:31234400-31257600	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr12:31234800-31252600	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr12:31235200-31246600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:31235200-31252000	Strong transcription	H9 Cell Line	embryonic stem cell
43	chr12:31235400-31246400	Strong transcription	Primary B cells from peripheral blood	blood
44	chr12:31235600-31239600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr12:31235600-31241800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr12:31235600-31242600	Strong transcription	Fetal Intestine Small	intestine
47	chr12:31235600-31242600	Strong transcription	Spleen	Spleen
48	chr12:31235600-31242800	Strong transcription	Fetal Stomach	stomach
49	chr12:31235600-31243000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr12:31235600-31243000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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