Variant report

Variant	esv2757495
Chromosome Location	chr12:31234168-31444218
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2686)
CpG islands
(count:1648)
Chromatin interactive
region (count:58)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31424813-31425127	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31399086-31399282	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31391820-31391981	K562	blood:	n/a	n/a
4	ATF1	chr12:31365662-31365782	K562	blood:	n/a	n/a
5	ATF1	chr12:31424834-31425154	K562	blood:	n/a	n/a
6	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
7	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr12:31432337-31432818	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
11	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
12	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
16	BATF	chr12:31434747-31435076	GM12878	blood:	n/a	n/a
17	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
18	BATF	chr12:31424868-31425107	GM12878	blood:	n/a	n/a
19	BATF	chr12:31434733-31435004	GM12878	blood:	n/a	n/a
20	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
21	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
22	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
23	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
25	BHLHE40	chr12:31418855-31418967	K562	blood:	n/a	n/a
26	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
28	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:31430083-31430222	K562	blood:	n/a	n/a
32	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:31424468-31424644	K562	blood:	n/a	n/a
34	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:31391842-31392078	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr12:31390019-31390036	GM12878	blood:	n/a	n/a
37	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
38	CBX3	chr12:31358885-31359398	HCT-116	colon:	n/a	n/a
39	CEBPB	chr12:31427493-31427774	A549	lung:	n/a	n/a
40	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:31424820-31425080	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr12:31355347-31355432	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
44	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
45	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
46	CEBPB	chr12:31395234-31395493	IMR90	lung:	n/a	n/a
47	CEBPB	chr12:31414835-31414948	K562	blood:	n/a	n/a
48	CEBPB	chr12:31391806-31392080	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
50	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31274424-31274474	GM19239	blood:	n/a
2	chr12:31274424-31274474	GM19239	blood:	n/a
3	chr12:31405359-31405409	AG10803	skin:	n/a
4	chr12:31274424-31274474	GM12891	blood:	n/a
5	chr12:31272865-31272915	HUVEC	blood vessel:	n/a
6	chr12:31272114-31272164	GM12878	blood:	n/a
7	chr12:31272112-31272162	HEK293	kidney:	embryo
8	chr12:31405499-31405549	HNPCEpiC	eye:	n/a
9	chr12:31256838-31256888	HCM	heart:	n/a
10	chr12:31271429-31271479	H1-hESC	embryonic stem cell:	embryo
11	chr12:31254007-31254057	NB4	blood:	n/a
12	chr12:31405499-31405549	SK-N-MC	brain:	n/a
13	chr12:31272119-31272169	SK-N-SH	brain:	n/a
14	chr12:31254007-31254057	H1-hESC	embryonic stem cell:	embryo
15	chr12:31254036-31254086	SK-N-MC	brain:	n/a
16	chr12:31272114-31272164	HRPEpiC	eye:	n/a
17	chr12:31378024-31378074	PFSK-1	brain:	n/a
18	chr12:31405499-31405549	PFSK-1	brain:	n/a
19	chr12:31272114-31272164	PANC-1	pancreas:	n/a
20	chr12:31432493-31432543	HCF	heart:	n/a
21	chr12:31254007-31254057	HEK293	kidney:	embryo
22	chr12:31412980-31413030	SK-N-MC	brain:	n/a
23	chr12:31272119-31272169	HMEC	breast:	n/a
24	chr12:31271783-31271833	NB4	blood:	n/a
25	chr12:31402470-31402520	GM12891	blood:	n/a
26	chr12:31370930-31370980	LNCaP	prostate:	n/a
27	chr12:31271429-31271479	LNCaP	prostate:	n/a
28	chr12:31274424-31274474	HCF	heart:	n/a
29	chr12:31241496-31241546	ECC-1	luminal epithelium:	n/a
30	chr12:31378024-31378074	RPTEC	kidney:	n/a
31	chr12:31405499-31405549	Jurkat	blood:	n/a
32	chr12:31254007-31254057	T-47D	breast:	n/a
33	chr12:31271783-31271833	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:31402470-31402520	IMR90	lung:	fetal
35	chr12:31271783-31271833	ProgFib	skin:	n/a
36	chr12:31271783-31271833	PANC-1	pancreas:	n/a
37	chr12:31272112-31272162	AoSMC	blood vessel:	n/a
38	chr12:31270326-31270376	H1-hESC	embryonic stem cell:	embryo
39	chr12:31405369-31405419	SKMC	muscle:	n/a
40	chr12:31254036-31254086	AG10803	skin:	n/a
41	chr12:31272865-31272915	NHBE	bronchial:	n/a
42	chr12:31254007-31254057	HCPEpiC	choroid plexus:	n/a
43	chr12:31276852-31276902	GM06990	blood:	n/a
44	chr12:31256838-31256888	SK-N-SH	brain:	n/a
45	chr12:31274424-31274474	HRCEpiC	kidney:	n/a
46	chr12:31412980-31413030	H1-hESC	embryonic stem cell:	embryo
47	chr12:31423331-31423381	AoSMC	blood vessel:	n/a
48	chr12:31272865-31272915	HIPEpiC	eye:	n/a
49	chr12:31412980-31413030	IMR90	lung:	fetal
50	chr12:31405359-31405409	ECC-1	luminal epithelium:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
2	chr12:31431393..31434433-chr12:31435348..31438398,4	K562	blood:
3	chr12:31388279..31391169-chr12:31396495..31398764,2	K562	blood:
4	chr12:31429753..31431642-chr12:31477161..31479179,2	MCF-7	breast:
5	chr12:31437269..31440946-chr12:31476584..31478708,4	K562	blood:
6	chr12:31431180..31432893-chr12:31435348..31438237,2	K562	blood:
7	chr12:31420076..31422123-chr12:31458375..31460920,2	K562	blood:
8	chr12:31433746..31435306-chr12:31477957..31479847,2	MCF-7	breast:
9	chr12:31431407..31434228-chr12:31440191..31441794,2	MCF-7	breast:
10	chr12:31440764..31443611-chr12:31446917..31448867,2	MCF-7	breast:
11	chr12:31424984..31425698-chr12:31516137..31516810,2	MCF-7	breast:
12	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
13	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
14	chr12:31405416..31405958-chr12:31422269..31422784,2	MCF-7	breast:
15	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
16	chr12:31269943..31270748-chr12:31391487..31392373,2	K562	blood:
17	chr12:31436681..31438944-chr12:31454544..31456802,2	K562	blood:
18	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
19	chr12:31358059..31360304-chr12:31368898..31371452,2	MCF-7	breast:
20	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
21	chr12:31406545..31409230-chr12:31409522..31411986,2	MCF-7	breast:
22	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
23	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
24	chr12:31442055..31443948-chr12:31476343..31479106,2	MCF-7	breast:
25	chr12:31431180..31432893-chr12:31435348..31438237,2	K562	blood:
26	chr12:31431393..31434433-chr12:31435348..31438398,4	K562	blood:
27	chr12:31404088..31405871-chr12:31424351..31425459,7	MCF-7	breast:
28	chr12:31442106..31444745-chr12:31447754..31449545,2	K562	blood:
29	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
30	chr12:31412613..31414977-chr12:31423446..31425840,2	K562	blood:
31	chr12:31426550..31428867-chr8:91672656..91674769,2	MCF-7	breast:
32	chr12:31438960..31441635-chr12:31476120..31479078,4	MCF-7	breast:
33	chr12:31427531..31430100-chr12:31477192..31479203,2	K562	blood:
34	chr12:31399111..31400912-chr12:31476871..31479529,2	MCF-7	breast:
35	chr12:31404333..31405560-chr12:31424545..31425415,3	K562	blood:
36	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
37	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
38	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
39	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
40	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
41	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
42	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
43	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
44	chr12:31441936..31444471-chr12:31461300..31463621,2	K562	blood:
45	chr12:31269317..31270662-chr12:31391620..31392355,3	MCF-7	breast:
46	chr12:31354464..31355986-chr12:31358238..31360954,2	K562	blood:
47	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
48	chr12:31412613..31414977-chr12:31423446..31425840,2	K562	blood:
49	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
50	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-2	chr12:31412950-31413502	ucscGeneNc_uc001rkg_2
2	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
3	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
4	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
5	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
6	lnc-AC024940.1-3	chr12:31397374-31397619	NONHSAT027541
7	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
8	lnc-FAM60A-2	chr12:31407684-31407996	ucscGeneNc_uc001rkg_2
9	lnc-FAM60A-4	chr12:31367135-31367371	expReg_chr12_2391_-

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM60A	hsa-miR-320a	chr12:31433853-31433872
2	FAM60A	hsa-miR-320a	chr12:31434102-31434124

Variant related genes	Relation type
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
ENSG00000270766	TF binding region
ENSG00000270395	TF binding region
ENSG00000243517	TF binding region
ENSG00000177359	TF binding region
DDX11	TF binding region
ENSG00000270926	CpG island
ENSG00000212533	CpG island
ENSG00000270766	CpG island
ENSG00000270395	CpG island
ENSG00000243517	CpG island
ENSG00000177359	CpG island
DDX11	CpG island
ENSG00000245614	chromatin interactions
ENSG00000270395	chromatin interactions
ENSG00000270766	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000177340	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000238661	chromatin interactions
ENSG00000243517	chromatin interactions

Extended variants
information (count: 6610 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6610 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11051237	chr12:31234168-31234169	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566405776	chr12:31234217-31234218	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536934375	chr12:31234224-31234225	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs4031340	chr12:31234229-31234230	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs548844357	chr12:31234231-31234232	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs570232041	chr12:31234236-31234237	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs4031341	chr12:31234240-31234241	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
8	rs4031342	chr12:31234274-31234275	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs559024976	chr12:31234282-31234283	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs577237476	chr12:31234308-31234309	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs4031343	chr12:31234312-31234313	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs534723769	chr12:31234320-31234321	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs188423448	chr12:31234329-31234330	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs4031344	chr12:31234344-31234345	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs373714075	chr12:31234392-31234393	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs2553154	chr12:31234442-31234443	Weak transcription Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs2553153	chr12:31234461-31234462	Weak transcription Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
18	rs534642589	chr12:31234486-31234487	Weak transcription Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs2553152	chr12:31234563-31234564	Weak transcription Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs144533890	chr12:31234599-31234600	Weak transcription Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs144453269	chr12:31234626-31234627	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2553151	chr12:31234732-31234733	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545647534	chr12:31234735-31234736	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564232128	chr12:31234747-31234748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528174751	chr12:31234777-31234778	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs61917209	chr12:31234781-31234782	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112310051	chr12:31234819-31234820	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185743164	chr12:31234917-31234918	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78071328	chr12:31234920-31234921	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs201775915	chr12:31234927-31234928	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199739640	chr12:31235064-31235065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71455612	chr12:31235078-31235079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2543264	chr12:31235106-31235107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201577383	chr12:31235199-31235200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199798687	chr12:31235231-31235232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200875125	chr12:31235281-31235282	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs2543265	chr12:31235296-31235297	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs4930951	chr12:31235354-31235355	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
39	rs537673542	chr12:31235368-31235369	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs4031323	chr12:31235371-31235372	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs4031324	chr12:31235378-31235379	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552472407	chr12:31235394-31235395	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs2553147	chr12:31235395-31235396	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs2553146	chr12:31235415-31235416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370395011	chr12:31235428-31235429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534786278	chr12:31235429-31235430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552998283	chr12:31235432-31235433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574496587	chr12:31235443-31235444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2553145	chr12:31235449-31235450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138425155	chr12:31235458-31235459	Weak transcription Strong transcription	n/a	n/a	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:2675 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227600-31235600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:31227600-31235800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:31227600-31236800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:31227600-31237000	Weak transcription	Aorta	Aorta
5	chr12:31227800-31235600	Weak transcription	Primary B cells from cord blood	blood
6	chr12:31227800-31235600	Weak transcription	Fetal Intestine Small	intestine
7	chr12:31227800-31235800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr12:31227800-31236000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr12:31227800-31236800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr12:31227800-31236800	Weak transcription	Brain Hippocampus Middle	brain
11	chr12:31227800-31237000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:31227800-31237000	Weak transcription	Gastric	stomach
13	chr12:31227800-31237000	Weak transcription	Lung	lung
14	chr12:31227800-31237000	Weak transcription	Right Ventricle	heart
15	chr12:31227800-31237400	Weak transcription	Ovary	ovary
16	chr12:31227800-31240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr12:31227800-31242000	Weak transcription	Left Ventricle	heart
18	chr12:31227800-31242600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
20	chr12:31228000-31234200	Weak transcription	Fetal Muscle Leg	muscle
21	chr12:31228000-31235200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr12:31228000-31235600	Weak transcription	Thymus	Thymus
23	chr12:31228000-31235800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:31228000-31235800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:31228000-31235800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr12:31228000-31235800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr12:31228000-31235800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr12:31228000-31236000	Weak transcription	Fetal Muscle Trunk	muscle
29	chr12:31228000-31236200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:31228000-31236600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr12:31228000-31236600	Weak transcription	Brain Germinal Matrix	brain
32	chr12:31228000-31236600	Weak transcription	Placenta	Placenta
33	chr12:31228000-31236800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr12:31228000-31236800	Weak transcription	Colonic Mucosa	Colon
35	chr12:31228000-31237000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:31228000-31237000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr12:31228000-31237000	Weak transcription	Adipose Nuclei	Adipose
38	chr12:31228000-31237000	Weak transcription	Brain Anterior Caudate	brain
39	chr12:31228000-31237000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr12:31228000-31237000	Weak transcription	Pancreas	Pancrea
41	chr12:31228000-31237000	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr12:31228000-31237000	Weak transcription	NHLF	lung
43	chr12:31228000-31237200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr12:31228000-31237600	Weak transcription	Fetal Lung	lung
45	chr12:31228000-31238200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr12:31228000-31242000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr12:31228000-31244400	Weak transcription	Fetal Kidney	kidney
48	chr12:31228000-31244600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:31228000-31249200	Weak transcription	Brain Angular Gyrus	brain
50	chr12:31228000-31255000	Weak transcription	Brain Cingulate Gyrus	brain

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