Variant report

Variant	nsv1036929
Chromosome Location	chr14:71469148-71683412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2313)
CpG islands
(count:918)
Chromatin interactive
region (count:67)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2313 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:71584599-71585049	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:71583321-71583963	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:71596906-71597822	K562	blood:	n/a	n/a
4	ARID3A	chr14:71610207-71610661	HepG2	liver:	n/a	n/a
5	ATF1	chr14:71597363-71597860	K562	blood:	n/a	n/a
6	ATF1	chr14:71609002-71609339	K562	blood:	n/a	n/a
7	ATF1	chr14:71610189-71610768	K562	blood:	n/a	n/a
8	ATF3	chr14:71648413-71648601	K562	blood:	n/a	n/a
9	ATF3	chr14:71610318-71610639	K562	blood:	n/a	n/a
10	ATF3	chr14:71488349-71488985	HCT-116	colon:	n/a	n/a
11	BATF	chr14:71678844-71679079	GM12878	blood:	n/a	n/a
12	BATF	chr14:71609226-71609612	GM12878	blood:	n/a	n/a
13	BATF	chr14:71678810-71679025	GM12878	blood:	n/a	n/a
14	BATF	chr14:71489604-71489981	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:71597411-71597742	GM12878	blood:	n/a	n/a
16	BCLAF1	chr14:71609019-71609668	GM12878	blood:	n/a	chr14:71609253-71609262
17	BHLHE40	chr14:71609976-71610290	HepG2	liver:	n/a	n/a
18	BHLHE40	chr14:71610027-71610482	K562	blood:	n/a	n/a
19	BHLHE40	chr14:71647954-71648314	K562	blood:	n/a	n/a
20	BHLHE40	chr14:71665607-71665710	K562	blood:	n/a	n/a
21	BHLHE40	chr14:71597583-71597614	GM12878	blood:	n/a	n/a
22	BHLHE40	chr14:71632108-71632438	K562	blood:	n/a	n/a
23	BHLHE40	chr14:71597213-71597764	K562	blood:	n/a	n/a
24	BRCA1	chr14:71501498-71501685	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr14:71541284-71541304	GM12878	blood:	n/a	n/a
26	BRCA1	chr14:71605864-71605925	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr14:71488393-71489537	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr14:71488110-71489423	HCT-116	colon:	n/a	n/a
29	CBX3	chr14:71545338-71545530	K562	blood:	n/a	n/a
30	CCNT2	chr14:71597368-71597644	K562	blood:	n/a	n/a
31	CEBPB	chr14:71529637-71529915	MCF-7	breast:	n/a	chr14:71529832-71529843
32	CEBPB	chr14:71585615-71585800	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:71632380-71632527	H1-hESC	embryonic stem cell:	n/a	chr14:71632446-71632457
34	CEBPB	chr14:71516332-71516714	A549	lung:	n/a	chr14:71516540-71516551
35	CEBPB	chr14:71561508-71561668	H1-hESC	embryonic stem cell:	n/a	chr14:71561598-71561609
36	CEBPB	chr14:71575532-71575809	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:71633175-71633508	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr14:71612709-71613024	HepG2	liver:	n/a	chr14:71612862-71612875 chr14:71612862-71612873
39	CEBPB	chr14:71488284-71489414	HCT-116	colon:	n/a	n/a
40	CEBPB	chr14:71529657-71529978	HepG2	liver:	n/a	chr14:71529832-71529843
41	CEBPB	chr14:71495934-71496677	HCT-116	colon:	n/a	n/a
42	CEBPB	chr14:71608478-71609776	IMR90	lung:	n/a	chr14:71609600-71609611 chr14:71609382-71609394 chr14:71609096-71609108
43	CEBPB	chr14:71607832-71608176	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:71527032-71527355	A549	lung:	n/a	chr14:71527177-71527188
45	CEBPB	chr14:71528197-71528501	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr14:71607823-71608165	IMR90	lung:	n/a	n/a
47	CEBPB	chr14:71584936-71586088	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr14:71511169-71511269	H1-hESC	embryonic stem cell:	n/a	chr14:71511242-71511253
49	CEBPB	chr14:71632296-71632622	K562	blood:	n/a	chr14:71632446-71632457
50	CEBPB	chr14:71657048-71657188	IMR90	lung:	n/a	chr14:71657146-71657157

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71472713-71472763	T-47D	breast:	n/a
2	chr14:71472713-71472763	HRE	kidney:	n/a
3	chr14:71609158-71609208	MCF-7	breast:	n/a
4	chr14:71472713-71472763	T-47D	breast:	n/a
5	chr14:71472713-71472763	HRE	kidney:	n/a
6	chr14:71609158-71609208	MCF-7	breast:	n/a
7	chr14:71515513-71515563	ovcar-3	ovarian:	n/a
8	chr14:71606274-71606324	HNPCEpiC	eye:	n/a
9	chr14:71598219-71598269	HEK293	kidney:	embryo
10	chr14:71585510-71585560	AG04450	lung:	fetal
11	chr14:71577479-71577529	HRCEpiC	kidney:	n/a
12	chr14:71598219-71598269	HCPEpiC	choroid plexus:	n/a
13	chr14:71581031-71581081	K562	blood:	n/a
14	chr14:71660200-71660250	HRPEpiC	eye:	n/a
15	chr14:71605994-71606044	BJ	skin:	n/a
16	chr14:71527576-71527626	PrEC	prostate:	n/a
17	chr14:71581031-71581081	AG10803	skin:	n/a
18	chr14:71555837-71555887	AoSMC	blood vessel:	n/a
19	chr14:71577479-71577529	NH-A	brain:	n/a
20	chr14:71555837-71555887	Hepatocyte	liver:	n/a
21	chr14:71577479-71577529	AG10803	skin:	n/a
22	chr14:71585510-71585560	GM06990	blood:	n/a
23	chr14:71472713-71472763	HCPEpiC	choroid plexus:	n/a
24	chr14:71606274-71606324	MCF10A-Er-Src	breast:	n/a
25	chr14:71606506-71606556	GM06990	blood:	n/a
26	chr14:71577479-71577529	Caco-2	colon:	n/a
27	chr14:71515513-71515563	SKMC	muscle:	n/a
28	chr14:71605994-71606044	Hepatocyte	liver:	n/a
29	chr14:71606506-71606556	HIPEpiC	eye:	n/a
30	chr14:71585510-71585560	Caco-2	colon:	n/a
31	chr14:71635288-71635338	HEK293	kidney:	embryo
32	chr14:71585510-71585560	HRPEpiC	eye:	n/a
33	chr14:71527576-71527626	K562	blood:	n/a
34	chr14:71635288-71635338	HAEpiC	amniotic membrane:	n/a
35	chr14:71577479-71577529	SAEC	small airway:	n/a
36	chr14:71609158-71609208	K562	blood:	n/a
37	chr14:71555837-71555887	HNPCEpiC	eye:	n/a
38	chr14:71606506-71606556	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:71515513-71515563	RPTEC	kidney:	n/a
40	chr14:71585510-71585560	HIPEpiC	eye:	n/a
41	chr14:71598219-71598269	SKMC	muscle:	n/a
42	chr14:71515513-71515563	HCT-116	colon:	n/a
43	chr14:71555837-71555887	HAEpiC	amniotic membrane:	n/a
44	chr14:71605994-71606044	HepG2	liver:	n/a
45	chr14:71632612-71632662	LNCaP	prostate:	n/a
46	chr14:71555837-71555887	IMR90	lung:	fetal
47	chr14:71632612-71632662	HIPEpiC	eye:	n/a
48	chr14:71605994-71606044	U87	brain:	n/a
49	chr14:71660200-71660250	NH-A	brain:	n/a
50	chr14:71606506-71606556	Hela-S3	cervix:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:71632939..71633847-chr14:71870165..71871025,2	MCF-7	breast:
2	chr14:71630664..71636301-chr14:71785635..71788811,7	MCF-7	breast:
3	chr14:71641459..71643782-chr14:71787456..71790205,2	MCF-7	breast:
4	chr14:71662526..71664078-chr14:71674837..71676717,2	K562	blood:
5	chr14:71570776..71571452-chr14:72219467..72220345,2	MCF-7	breast:
6	chr14:71472106..71474140-chr14:71476821..71478999,2	K562	blood:
7	chr14:71609565..71610435-chr14:73603108..73603774,2	Hela-S3	cervix:
8	chr14:71570510..71571060-chr14:71673984..71674688,2	K562	blood:
9	chr14:71570510..71571060-chr14:71673984..71674688,2	K562	blood:
10	chr14:71673509..71676275-chr14:71679068..71681548,4	MCF-7	breast:
11	chr14:71605403..71606379-chr14:72219242..72220271,11	MCF-7	breast:
12	chr14:71540159..71540880-chr9:91932962..91933924,2	NB4	blood:
13	chr14:71576318..71579821-chr14:71580472..71584172,4	MCF-7	breast:
14	chr14:71632877..71633633-chr14:71789090..71789926,3	MCF-7	breast:
15	chr14:71605416..71606618-chr14:72219460..72220340,5	MCF-7	breast:
16	chr14:71643231..71645889-chr14:72138458..72140517,2	MCF-7	breast:
17	chr14:71653618..71655729-chr14:71657519..71659044,2	MCF-7	breast:
18	chr14:71580577..71583944-chr14:71584359..71586589,3	K562	blood:
19	chr14:71570663..71571191-chr14:72219553..72220390,2	MCF-7	breast:
20	chr14:71666330..71668532-chr14:71673021..71675504,2	MCF-7	breast:
21	chr14:71605592..71606386-chr14:71869586..71870379,2	MCF-7	breast:
22	chr14:71604707..71606600-chr14:72213499..72215384,2	MCF-7	breast:
23	chr14:71608562..71610263-chr14:71786915..71789760,2	MCF-7	breast:
24	chr14:71610357..71611926-chr14:71786839..71789393,2	MCF-7	breast:
25	chr14:71678893..71680669-chr14:71681076..71683305,2	MCF-7	breast:
26	chr14:71629289..71631183-chr14:71936634..71939360,2	MCF-7	breast:
27	chr14:71607200..71607876-chr14:72219653..72220319,2	MCF-7	breast:
28	chr14:71521439..71523990-chr14:71537038..71539301,2	MCF-7	breast:
29	chr14:71662526..71664078-chr14:71674837..71676717,2	K562	blood:
30	chr14:71536680..71538584-chr14:71630559..71632306,2	MCF-7	breast:
31	chr14:71511687..71514106-chr14:71519945..71521504,2	MCF-7	breast:
32	chr14:71576010..71578175-chr14:71578987..71581734,2	K562	blood:
33	chr14:71652746..71656489-chr14:71786272..71789220,3	MCF-7	breast:
34	chr14:71652798..71655797-chr14:71786372..71789241,2	MCF-7	breast:
35	chr14:71487547..71489766-chr14:72170994..72172928,2	MCF-7	breast:
36	chr14:71511687..71514106-chr14:71519945..71521504,2	MCF-7	breast:
37	chr14:71640952..71644715-chr14:71785827..71788552,4	MCF-7	breast:
38	chr14:71647115..71649453-chr14:71786412..71788278,2	MCF-7	breast:
39	chr14:71179105..71181314-chr14:71570757..71573577,2	K562	blood:
40	chr14:71487162..71488929-chr14:71491873..71493814,2	MCF-7	breast:
41	chr14:71570724..71571280-chr14:72321914..72322593,2	K562	blood:
42	chr14:71576318..71579821-chr14:71580472..71584172,4	MCF-7	breast:
43	chr14:71496994..71499814-chr14:71507368..71509896,2	MCF-7	breast:
44	chr14:71633208..71633853-chr14:71776471..71777116,3	MCF-7	breast:
45	chr14:71604769..71607668-chr14:71786929..71789620,2	MCF-7	breast:
46	chr14:71576010..71578175-chr14:71578987..71581734,2	K562	blood:
47	chr14:71521439..71523990-chr14:71537038..71539301,2	MCF-7	breast:
48	chr14:71624159..71626402-chr14:71786636..71788555,2	MCF-7	breast:
49	chr14:71273334..71275325-chr14:71487514..71489742,2	MCF-7	breast:
50	chr14:71633131..71633707-chr14:71787970..71788477,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCNX-3	chr14:71679350-71679659	ENSG00000258517
2	lnc-MAP3K9-9	chr14:71552199-71552550	NONHSAT037605
3	lnc-SIPA1L1-5	chr14:71581486-71582098	NONHSAT037606
4	lnc-MAP3K9-7	chr14:71498403-71498687	NONHSAT037603
5	lnc-PCNX-1	chr14:71648173-71648823	ENSG00000259907.1
6	lnc-PCNX-1	chr14:71648069-71648822	NONHSAT037608
7	lnc-PCNX-1	chr14:71647678-71647919	NONHSAT037608
8	lnc-MAP3K9-8	chr14:71511092-71511357	NONHSAT037604
9	lnc-MAP3K9-1	chr14:71648070-71648822	XLOC_011063
10	lnc-MAP3K9-1	chr14:71647679-71647919	XLOC_011063
11	lnc-MAP3K9-10	chr14:71607842-71609970	ENSG00000269927.1

No data

Variant related genes	Relation type
PCNX	TF binding region
ENSG00000258930	TF binding region
ENSG00000259907	TF binding region
ENSG00000269945	TF binding region
ENSG00000269927	TF binding region
PTTG4P	TF binding region
ENSG00000258517	TF binding region
ENSG00000258966	TF binding region
PCNX	CpG island
ENSG00000258930	CpG island
ENSG00000259907	CpG island
ENSG00000269945	CpG island
ENSG00000269927	CpG island
PTTG4P	CpG island
ENSG00000258517	CpG island
ENSG00000258966	CpG island
ENSG00000259146	chromatin interactions
ENSG00000080815	chromatin interactions
ENSG00000100731	chromatin interactions
ENSG00000258517	chromatin interactions
ENSG00000197555	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000259907	chromatin interactions
ENSG00000258930	chromatin interactions

Extended variants
information (count: 8002 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:8002 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56370042	chr14:71469152-71469153	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188521394	chr14:71469155-71469156	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs181610586	chr14:71469165-71469166	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547623230	chr14:71469236-71469237	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs79883357	chr14:71469290-71469291	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs557554634	chr14:71469336-71469337	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs9323555	chr14:71469380-71469381	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs12433409	chr14:71469420-71469421	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554312335	chr14:71469453-71469454	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs35561518	chr14:71469485-71469486	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs9323556	chr14:71469512-71469513	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs558254670	chr14:71469513-71469514	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs576497728	chr14:71469528-71469529	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs78470952	chr14:71469535-71469536	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs562324040	chr14:71469594-71469595	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs552695077	chr14:71469634-71469635	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529991146	chr14:71469680-71469681	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542099057	chr14:71469699-71469700	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560148879	chr14:71469727-71469728	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149014460	chr14:71469755-71469756	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546987128	chr14:71469756-71469757	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370428666	chr14:71469789-71469790	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs71448340	chr14:71469790-71469791	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371644226	chr14:71469792-71469793	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373310824	chr14:71469794-71469795	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377019884	chr14:71469797-71469798	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571785715	chr14:71469800-71469801	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs3083307	chr14:71469817-71469818	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111548108	chr14:71469823-71469824	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186981134	chr14:71469904-71469905	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551222233	chr14:71469923-71469924	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2332506	chr14:71469924-71469925	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs536582664	chr14:71469972-71469973	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191811644	chr14:71469973-71469974	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182267685	chr14:71470059-71470060	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368753137	chr14:71470060-71470061	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77039754	chr14:71470064-71470065	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187286295	chr14:71470072-71470073	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576561108	chr14:71470073-71470074	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140064981	chr14:71470100-71470101	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200189160	chr14:71470222-71470223	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555981198	chr14:71470250-71470251	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574585796	chr14:71470255-71470256	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150324964	chr14:71470335-71470336	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560418057	chr14:71470404-71470405	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs137972535	chr14:71470431-71470432	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143517668	chr14:71470461-71470462	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565256555	chr14:71470498-71470499	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532697176	chr14:71470510-71470511	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551082708	chr14:71470529-71470530	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4897 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71426000-71508800	Weak transcription	Psoas Muscle	Psoas
2	chr14:71437200-71485600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:71438600-71502800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:71439200-71478000	Weak transcription	Colon Smooth Muscle	Colon
5	chr14:71439600-71502800	Weak transcription	Small Intestine	intestine
6	chr14:71445200-71470800	Weak transcription	GM12878-XiMat	blood
7	chr14:71445200-71471000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:71445200-71496200	Weak transcription	Fetal Brain Male	brain
9	chr14:71445200-71497800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr14:71445200-71502800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:71445200-71510800	Weak transcription	Colonic Mucosa	Colon
12	chr14:71445400-71470600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:71445400-71470600	Weak transcription	Fetal Stomach	stomach
14	chr14:71445400-71470800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:71445400-71471000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr14:71445400-71471000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr14:71445400-71471000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr14:71445400-71479600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr14:71445400-71479800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr14:71445400-71479800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr14:71445400-71479800	Weak transcription	Thymus	Thymus
22	chr14:71445400-71479800	Weak transcription	HSMMtube	muscle
23	chr14:71445400-71480400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr14:71445400-71480400	Weak transcription	Left Ventricle	heart
25	chr14:71445400-71485600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr14:71445400-71498000	Weak transcription	Brain Hippocampus Middle	brain
27	chr14:71445400-71502800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr14:71445600-71477400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr14:71445600-71477600	Weak transcription	Adipose Nuclei	Adipose
30	chr14:71445600-71479800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr14:71445600-71479800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr14:71445800-71471800	Weak transcription	Fetal Muscle Leg	muscle
33	chr14:71446200-71470800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:71447000-71471200	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr14:71447800-71479800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr14:71448000-71479800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr14:71448000-71485800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr14:71449000-71470800	Weak transcription	NHDF-Ad	bronchial
39	chr14:71449600-71470800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr14:71453400-71471000	Weak transcription	HUVEC	blood vessel
41	chr14:71454600-71480400	Weak transcription	Brain Angular Gyrus	brain
42	chr14:71455400-71470800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr14:71455600-71470800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr14:71455600-71471600	Weak transcription	Duodenum Mucosa	Duodenum
45	chr14:71455600-71479800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:71455600-71497400	Weak transcription	Right Ventricle	heart
47	chr14:71456200-71470600	Weak transcription	NHLF	lung
48	chr14:71456800-71478800	Weak transcription	Fetal Lung	lung
49	chr14:71458400-71470800	Weak transcription	Fetal Intestine Large	intestine
50	chr14:71460200-71480600	Weak transcription	Brain Anterior Caudate	brain

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