Variant report

Variant	nsv1043187
Chromosome Location	chr12:31356144-31444060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1736)
CpG islands
(count:672)
Chromatin interactive
region (count:54)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr12:31424834-31425154	K562	blood:	n/a	n/a
5	ATF1	chr12:31365662-31365782	K562	blood:	n/a	n/a
6	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
7	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
9	ATF2	chr12:31432337-31432818	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
13	BATF	chr12:31424868-31425107	GM12878	blood:	n/a	n/a
14	BATF	chr12:31434747-31435076	GM12878	blood:	n/a	n/a
15	BATF	chr12:31434733-31435004	GM12878	blood:	n/a	n/a
16	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
17	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
19	BHLHE40	chr12:31418855-31418967	K562	blood:	n/a	n/a
20	BHLHE40	chr12:31424468-31424644	K562	blood:	n/a	n/a
21	BHLHE40	chr12:31430083-31430222	K562	blood:	n/a	n/a
22	BRCA1	chr12:31391842-31392078	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr12:31390019-31390036	GM12878	blood:	n/a	n/a
24	CBX3	chr12:31358885-31359398	HCT-116	colon:	n/a	n/a
25	CEBPB	chr12:31395234-31395493	IMR90	lung:	n/a	n/a
26	CEBPB	chr12:31424820-31425080	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr12:31391806-31392080	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:31414835-31414948	K562	blood:	n/a	n/a
29	CEBPB	chr12:31427540-31427765	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:31401830-31402026	HepG2	liver:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
31	CEBPB	chr12:31395273-31395514	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:31401823-31402021	Hela-S3	cervix:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
33	CEBPB	chr12:31427493-31427774	A549	lung:	n/a	n/a
34	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
35	CEBPB	chr12:31391866-31392108	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr12:31436720-31436759	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr12:31432406-31433417	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr12:31371770-31371778	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr12:31358885-31359207	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr12:31424765-31425200	H1-hESC	embryonic stem cell:	n/a	chr12:31424980-31424993
41	CREB1	chr12:31424733-31425219	H1-hESC	embryonic stem cell:	n/a	chr12:31424980-31424993
42	CTCF	chr12:31404280-31404430	NB4	blood:	n/a	n/a
43	CTCF	chr12:31405020-31405170	AG04450	lung:	n/a	n/a
44	CTCF	chr12:31424900-31425050	HepG2	liver:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
45	CTCF	chr12:31424836-31425299	K562	blood:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
46	CTCF	chr12:31424920-31425070	HPAF	blood vessel:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
47	CTCF	chr12:31424918-31425143	GM19238	blood:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
48	CTCF	chr12:31398976-31399381	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:31368669-31368796	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:31368700-31368850	GM12873	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31432493-31432543	PFSK-1	brain:	n/a
2	chr12:31432493-31432543	PFSK-1	brain:	n/a
3	chr12:31405369-31405419	GM19239	blood:	n/a
4	chr12:31405369-31405419	GM06990	blood:	n/a
5	chr12:31405359-31405409	Hela-S3	cervix:	n/a
6	chr12:31370930-31370980	AG04450	lung:	fetal
7	chr12:31370930-31370980	HepG2	liver:	n/a
8	chr12:31406441-31406491	Caco-2	colon:	n/a
9	chr12:31402470-31402520	PrEC	prostate:	n/a
10	chr12:31405359-31405409	CMK	blood:	n/a
11	chr12:31405369-31405419	SK-N-SH_RA	brain:	n/a
12	chr12:31405499-31405549	T-47D	breast:	n/a
13	chr12:31402470-31402520	MCF-7	breast:	n/a
14	chr12:31405369-31405419	SAEC	small airway:	n/a
15	chr12:31412980-31413030	AG04449	skin:	fetal
16	chr12:31406441-31406491	HAEpiC	amniotic membrane:	n/a
17	chr12:31405499-31405549	NHDF-neo	bronchial:	n/a
18	chr12:31412980-31413030	HCPEpiC	choroid plexus:	n/a
19	chr12:31360362-31360412	AG09309	skin:	n/a
20	chr12:31406441-31406491	GM06990	blood:	n/a
21	chr12:31406441-31406491	T-47D	breast:	n/a
22	chr12:31405359-31405409	GM19239	blood:	n/a
23	chr12:31412980-31413030	HCT-116	colon:	n/a
24	chr12:31405499-31405549	ovcar-3	ovarian:	n/a
25	chr12:31370930-31370980	K562	blood:	n/a
26	chr12:31423331-31423381	SK-N-MC	brain:	n/a
27	chr12:31406441-31406491	LNCaP	prostate:	n/a
28	chr12:31432493-31432543	NH-A	brain:	n/a
29	chr12:31378024-31378074	SK-N-SH_RA	brain:	n/a
30	chr12:31423331-31423381	PANC-1	pancreas:	n/a
31	chr12:31370930-31370980	NT2-D1	testis:	n/a
32	chr12:31370930-31370980	HEEpiC	esophagus:	n/a
33	chr12:31405359-31405409	H1-hESC	embryonic stem cell:	embryo
34	chr12:31423331-31423381	MCF10A-Er-Src	breast:	n/a
35	chr12:31360362-31360412	NT2-D1	testis:	n/a
36	chr12:31432493-31432543	K562	blood:	n/a
37	chr12:31378024-31378074	HRPEpiC	eye:	n/a
38	chr12:31378024-31378074	HUVEC	blood vessel:	n/a
39	chr12:31423331-31423381	HAEpiC	amniotic membrane:	n/a
40	chr12:31423331-31423381	GM12891	blood:	n/a
41	chr12:31370930-31370980	HUVEC	blood vessel:	n/a
42	chr12:31378024-31378074	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:31370930-31370980	SK-N-SH_RA	brain:	n/a
44	chr12:31402470-31402520	HCM	heart:	n/a
45	chr12:31432493-31432543	HRPEpiC	eye:	n/a
46	chr12:31423331-31423381	AG04449	skin:	fetal
47	chr12:31370930-31370980	PANC-1	pancreas:	n/a
48	chr12:31378024-31378074	SK-N-SH	brain:	n/a
49	chr12:31405359-31405409	IMR90	lung:	fetal
50	chr12:31412980-31413030	ProgFib	skin:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:31406545..31409230-chr12:31409522..31411986,2	MCF-7	breast:
2	chr12:31431393..31434433-chr12:31435348..31438398,4	K562	blood:
3	chr12:31431393..31434433-chr12:31435348..31438398,4	K562	blood:
4	chr12:31431407..31434228-chr12:31440191..31441794,2	MCF-7	breast:
5	chr12:31431407..31434228-chr12:31440191..31441794,2	MCF-7	breast:
6	chr12:31412613..31414977-chr12:31423446..31425840,2	K562	blood:
7	chr12:31399111..31400912-chr12:31476871..31479529,2	MCF-7	breast:
8	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
9	chr12:31404333..31405560-chr12:31424545..31425415,3	K562	blood:
10	chr12:31424984..31425698-chr12:31516137..31516810,2	MCF-7	breast:
11	chr12:31442055..31443948-chr12:31476343..31479106,2	MCF-7	breast:
12	chr12:31405416..31405958-chr12:31422269..31422784,2	MCF-7	breast:
13	chr12:31431180..31432893-chr12:31435348..31438237,2	K562	blood:
14	chr12:31427531..31430100-chr12:31477192..31479203,2	K562	blood:
15	chr12:31391273..31391961-chr12:31404788..31405659,2	K562	blood:
16	chr12:31431180..31432893-chr12:31435348..31438237,2	K562	blood:
17	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
18	chr12:31429753..31431642-chr12:31477161..31479179,2	MCF-7	breast:
19	chr12:30999874..31000492-chr12:31398859..31399728,2	K562	blood:
20	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
21	chr12:31269781..31270824-chr12:31398705..31400061,4	MCF-7	breast:
22	chr12:31433746..31435306-chr12:31477957..31479847,2	MCF-7	breast:
23	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
24	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
25	chr12:31388279..31391169-chr12:31396495..31398764,2	K562	blood:
26	chr12:31269317..31270662-chr12:31391620..31392355,3	MCF-7	breast:
27	chr12:31440764..31443611-chr12:31446917..31448867,2	MCF-7	breast:
28	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
29	chr12:31420076..31422123-chr12:31458375..31460920,2	K562	blood:
30	chr12:31412613..31414977-chr12:31423446..31425840,2	K562	blood:
31	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
32	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
33	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
34	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
35	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
36	chr12:31441936..31444471-chr12:31461300..31463621,2	K562	blood:
37	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
38	chr12:31442106..31444745-chr12:31447754..31449545,2	K562	blood:
39	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
40	chr12:31438960..31441635-chr12:31476120..31479078,4	MCF-7	breast:
41	chr12:31426550..31428867-chr8:91672656..91674769,2	MCF-7	breast:
42	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
43	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
44	chr12:31404088..31405871-chr12:31424351..31425459,7	MCF-7	breast:
45	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
46	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
47	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
48	chr12:31437269..31440946-chr12:31476584..31478708,4	K562	blood:
49	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
50	chr12:31269943..31270748-chr12:31391487..31392373,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-2	chr12:31407684-31407996	ucscGeneNc_uc001rkg_2
2	lnc-FAM60A-4	chr12:31367135-31367371	expReg_chr12_2391_-
3	lnc-FAM60A-2	chr12:31412950-31413502	ucscGeneNc_uc001rkg_2
4	lnc-AC024940.1-3	chr12:31397374-31397619	NONHSAT027541

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
ENSG00000243517	TF binding region
ENSG00000177359	TF binding region
ENSG00000270766	TF binding region
ENSG00000270395	TF binding region
ENSG00000243517	CpG island
ENSG00000177359	CpG island
ENSG00000270766	CpG island
ENSG00000270395	CpG island
ENSG00000139146	chromatin interactions
ENSG00000238661	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000270766	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000177340	chromatin interactions
ENSG00000270395	chromatin interactions

Extended variants
information (count: 3607 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3607 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150060694	chr12:31356153-31356154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180704841	chr12:31356255-31356256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563222934	chr12:31356259-31356260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530749785	chr12:31356261-31356262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568279777	chr12:31356287-31356288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537278994	chr12:31356341-31356342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550872508	chr12:31356355-31356356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570704563	chr12:31356367-31356368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548760763	chr12:31356497-31356498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539811245	chr12:31356544-31356545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76876048	chr12:31356547-31356548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77467656	chr12:31356550-31356551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186271697	chr12:31356574-31356575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555504170	chr12:31356683-31356684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575416454	chr12:31356708-31356709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200234766	chr12:31356711-31356712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199920851	chr12:31356714-31356715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368524866	chr12:31356784-31356785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544428637	chr12:31356800-31356801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533599510	chr12:31356822-31356823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551968791	chr12:31356827-31356828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528993910	chr12:31356874-31356875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564795876	chr12:31356885-31356886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4931454	chr12:31356893-31356894	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs35172070	chr12:31356914-31356915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12311267	chr12:31356929-31356930	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs559109696	chr12:31356969-31356970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528155854	chr12:31357023-31357024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553009772	chr12:31357087-31357088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10492354	chr12:31357102-31357103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs558977556	chr12:31357108-31357109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115433294	chr12:31357170-31357171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145408663	chr12:31357189-31357190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149588849	chr12:31357258-31357259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs59053182	chr12:31357271-31357272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538649438	chr12:31357272-31357273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570685628	chr12:31357274-31357275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539354054	chr12:31357303-31357304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546944514	chr12:31357471-31357472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372977104	chr12:31357487-31357488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79440212	chr12:31357608-31357609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114179278	chr12:31357625-31357626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11051321	chr12:31357664-31357665	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs575324252	chr12:31357698-31357699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35950278	chr12:31357742-31357743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114098924	chr12:31357757-31357758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1907698	chr12:31357820-31357821	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs146412085	chr12:31357870-31357871	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs75645575	chr12:31357893-31357894	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs558075213	chr12:31357912-31357913	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1211 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31355200-31362600	Enhancers	HMEC	breast
2	chr12:31355800-31356400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr12:31356000-31356400	Enhancers	Primary B cells from peripheral blood	blood
4	chr12:31356000-31356400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:31356000-31356600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:31356000-31356600	Enhancers	Primary T cells from cord blood	blood
7	chr12:31356000-31357000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:31356200-31356400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:31356200-31356800	Enhancers	NHEK	skin
10	chr12:31356400-31356800	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr12:31356400-31357600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:31356400-31358000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:31356400-31360800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:31356600-31357600	Weak transcription	Primary T cells from cord blood	blood
15	chr12:31356600-31358200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr12:31356600-31360400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr12:31356800-31357200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr12:31356800-31357200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:31356800-31357800	Weak transcription	NHEK	skin
20	chr12:31357000-31358200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:31357000-31360400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr12:31357000-31360600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:31357200-31359000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr12:31357200-31359000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:31357600-31358400	Enhancers	Primary B cells from peripheral blood	blood
26	chr12:31357600-31358400	Enhancers	Primary T cells from cord blood	blood
27	chr12:31357600-31358400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:31357600-31358600	Enhancers	Primary B cells from cord blood	blood
29	chr12:31357800-31358000	Active TSS	GM12878-XiMat	blood
30	chr12:31357800-31359400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr12:31357800-31362000	Enhancers	NHEK	skin
32	chr12:31358000-31358200	Enhancers	Duodenum Mucosa	Duodenum
33	chr12:31358000-31358200	Enhancers	GM12878-XiMat	blood
34	chr12:31358000-31358400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr12:31358000-31358400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr12:31358000-31358400	Enhancers	Adipose Nuclei	Adipose
37	chr12:31358000-31358400	Enhancers	HSMM	muscle
38	chr12:31358000-31358600	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr12:31358000-31359600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:31358000-31359600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr12:31358000-31359600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:31358000-31360000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:31358000-31360600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr12:31358000-31361800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:31358200-31358400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:31358200-31358400	Flanking Active TSS	GM12878-XiMat	blood
47	chr12:31358200-31359600	Enhancers	HSMMtube	muscle
48	chr12:31358200-31360200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr12:31358200-31362200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:31358400-31358800	Weak transcription	H9 Cell Line	embryonic stem cell

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