Variant report

Variant	nsv456346
Chromosome Location	chr14:81399692-81448382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:968)
CpG islands
(count:1588)
Chromatin interactive
region (count:35)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81407660-81407725	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:81421092-81421441	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:81421155-81421357	K562	blood:	n/a	n/a
4	ARID3A	chr14:81408038-81408468	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:81408108-81408383	K562	blood:	n/a	n/a
6	ATF2	chr14:81425656-81426351	GM12878	blood:	n/a	n/a
7	ATF2	chr14:81425667-81426340	GM12878	blood:	n/a	n/a
8	BACH1	chr14:81421226-81421524	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:81407866-81408111	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:81407987-81408051	K562	blood:	n/a	n/a
11	BACH1	chr14:81422602-81422695	K562	blood:	n/a	n/a
12	BACH1	chr14:81421988-81422007	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr14:81406533-81406767	GM12878	blood:	n/a	chr14:81406669-81406679 chr14:81406668-81406679
14	BATF	chr14:81425713-81426251	GM12878	blood:	n/a	n/a
15	BATF	chr14:81425702-81426242	GM12878	blood:	n/a	n/a
16	BCL11A	chr14:81425717-81426288	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
17	BCL11A	chr14:81425794-81426232	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
18	BCLAF1	chr14:81425680-81426248	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
19	BCLAF1	chr14:81407837-81408461	GM12878	blood:	n/a	n/a
20	BCLAF1	chr14:81407906-81408368	GM12878	blood:	n/a	n/a
21	BCLAF1	chr14:81425756-81426310	GM12878	blood:	n/a	chr14:81425939-81425948 chr14:81426062-81426070
22	BCLAF1	chr14:81421043-81421453	GM12878	blood:	n/a	chr14:81421296-81421309
23	BHLHE40	chr14:81407974-81408354	GM12878	blood:	n/a	n/a
24	BHLHE40	chr14:81407612-81408380	K562	blood:	n/a	n/a
25	BHLHE40	chr14:81421148-81421499	K562	blood:	n/a	chr14:81421348-81421364
26	BHLHE40	chr14:81408033-81408295	HepG2	liver:	n/a	n/a
27	BHLHE40	chr14:81425723-81426256	GM12878	blood:	n/a	n/a
28	BRCA1	chr14:81408192-81408491	HepG2	liver:	n/a	n/a
29	BRCA1	chr14:81407519-81408600	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr14:81407957-81408768	GM12878	blood:	n/a	n/a
31	BRCA1	chr14:81421111-81421414	H1-hESC	embryonic stem cell:	n/a	n/a
32	CCNT2	chr14:81421175-81421533	K562	blood:	n/a	n/a
33	CEBPB	chr14:81442099-81442223	H1-hESC	embryonic stem cell:	n/a	chr14:81442185-81442196
34	CEBPB	chr14:81442064-81442271	ECC-1	luminal epithelium:	n/a	chr14:81442185-81442196
35	CEBPB	chr14:81408084-81408212	K562	blood:	n/a	n/a
36	CEBPB	chr14:81432300-81432458	A549	lung:	n/a	n/a
37	CEBPB	chr14:81441925-81442291	MCF-7	breast:	n/a	chr14:81442185-81442196
38	CEBPB	chr14:81438173-81438481	IMR90	lung:	n/a	n/a
39	CEBPB	chr14:81442040-81442209	HepG2	liver:	n/a	chr14:81442185-81442196
40	CEBPB	chr14:81442015-81442295	MCF-7	breast:	n/a	chr14:81442185-81442196
41	CEBPB	chr14:81421099-81421425	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr14:81440617-81441103	ECC-1	luminal epithelium:	n/a	chr14:81440878-81440891
43	CEBPB	chr14:81411593-81411942	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:81411575-81411956	IMR90	lung:	n/a	n/a
45	CEBPB	chr14:81411638-81411887	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr14:81411597-81411900	K562	blood:	n/a	n/a
47	CEBPB	chr14:81411632-81411788	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr14:81425893-81426171	GM12878	blood:	n/a	n/a
49	CEBPB	chr14:81411592-81411951	A549	lung:	n/a	n/a
50	CEBPB	chr14:81408021-81408292	HepG2	liver:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81407087-81407137	HUVEC	blood vessel:	n/a
2	chr14:81407087-81407137	U87	brain:	n/a
3	chr14:81407087-81407137	HUVEC	blood vessel:	n/a
4	chr14:81407087-81407137	U87	brain:	n/a
5	chr14:81425912-81425962	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:81405846-81405896	HEK293	kidney:	embryo
7	chr14:81422098-81422148	GM12892	blood:	n/a
8	chr14:81421983-81422033	HCT-116	colon:	n/a
9	chr14:81421322-81421372	Caco-2	colon:	n/a
10	chr14:81421983-81422033	MCF10A-Er-Src	breast:	n/a
11	chr14:81421403-81421453	SK-N-SH_RA	brain:	n/a
12	chr14:81422111-81422161	HRCEpiC	kidney:	n/a
13	chr14:81421403-81421453	SKMC	muscle:	n/a
14	chr14:81425912-81425962	NHDF-neo	bronchial:	n/a
15	chr14:81426234-81426284	A549	lung:	n/a
16	chr14:81422160-81422210	GM06990	blood:	n/a
17	chr14:81408124-81408174	HepG2	liver:	n/a
18	chr14:81424527-81424577	AG04449	skin:	fetal
19	chr14:81422160-81422210	K562	blood:	n/a
20	chr14:81421763-81421813	AG10803	skin:	n/a
21	chr14:81408086-81408136	Caco-2	colon:	n/a
22	chr14:81425912-81425962	A549	lung:	n/a
23	chr14:81408124-81408174	SK-N-MC	brain:	n/a
24	chr14:81421983-81422033	HRCEpiC	kidney:	n/a
25	chr14:81421403-81421453	HMEC	breast:	n/a
26	chr14:81424527-81424577	NH-A	brain:	n/a
27	chr14:81407988-81408038	HL-60	blood:	n/a
28	chr14:81408124-81408174	NHDF-neo	bronchial:	n/a
29	chr14:81408086-81408136	IMR90	lung:	fetal
30	chr14:81422098-81422148	PrEC	prostate:	n/a
31	chr14:81407087-81407137	GM06990	blood:	n/a
32	chr14:81425912-81425962	H1-hESC	embryonic stem cell:	embryo
33	chr14:81407711-81407761	HUVEC	blood vessel:	n/a
34	chr14:81421322-81421372	AG04449	skin:	fetal
35	chr14:81421297-81421347	A549	lung:	n/a
36	chr14:81421770-81421820	RPTEC	kidney:	n/a
37	chr14:81404956-81405006	AG10803	skin:	n/a
38	chr14:81422098-81422148	A549	lung:	n/a
39	chr14:81421600-81421650	NH-A	brain:	n/a
40	chr14:81408275-81408325	HRCEpiC	kidney:	n/a
41	chr14:81421763-81421813	U87	brain:	n/a
42	chr14:81421983-81422033	MCF-7	breast:	n/a
43	chr14:81421763-81421813	PANC-1	pancreas:	n/a
44	chr14:81422160-81422210	Caco-2	colon:	n/a
45	chr14:81422111-81422161	HAEpiC	amniotic membrane:	n/a
46	chr14:81426577-81426627	ECC-1	luminal epithelium:	n/a
47	chr14:81425912-81425962	HAEpiC	amniotic membrane:	n/a
48	chr14:81404956-81405006	H1-hESC	embryonic stem cell:	embryo
49	chr14:81425912-81425962	Hela-S3	cervix:	n/a
50	chr14:81404956-81405006	Hela-S3	cervix:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81396675..81399080-chr14:81400094..81402837,4	K562	blood:
2	chr14:81406001..81408090-chr14:81684696..81687286,2	MCF-7	breast:
3	chr14:81442891..81446024-chr14:81447547..81451295,3	K562	blood:
4	chr14:81421633..81424276-chr14:81426151..81427849,2	K562	blood:
5	chr14:81429871..81432242-chr14:81433461..81436310,2	MCF-7	breast:
6	chr14:81443218..81445707-chr14:81448649..81450326,2	K562	blood:
7	chr14:81405781..81407858-chr14:81414654..81417606,2	K562	blood:
8	chr14:81434370..81436740-chr14:81683438..81686246,2	MCF-7	breast:
9	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:
10	chr14:81400340..81402827-chr14:81422342..81424603,2	K562	blood:
11	chr14:81432696..81434242-chr14:81439337..81441996,2	MCF-7	breast:
12	chr14:81413969..81417033-chr14:81418099..81421076,3	K562	blood:
13	chr14:81427260..81428823-chr14:81430386..81432233,2	MCF-7	breast:
14	chr14:81437706..81439686-chr14:81442892..81444755,2	MCF-7	breast:
15	chr14:81401530..81405637-chr14:81405681..81409826,5	K562	blood:
16	chr14:81400340..81402827-chr14:81422342..81424603,2	K562	blood:
17	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:
18	chr14:81427520..81429022-chr14:81432254..81434626,2	K562	blood:
19	chr14:81396050..81399080-chr14:81399956..81402754,3	K562	blood:
20	chr14:81413969..81417033-chr14:81418099..81421076,3	K562	blood:
21	chr14:81427520..81429022-chr14:81432254..81434626,2	K562	blood:
22	chr14:81409086..81412079-chr14:81684654..81686943,2	K562	blood:
23	chr14:81420793..81423189-chr14:81424553..81427836,4	MCF-7	breast:
24	chr14:81397911..81402411-chr14:81683829..81688491,5	K562	blood:
25	chr14:81429469..81431335-chr14:81685731..81687718,2	K562	blood:
26	chr14:81437706..81439686-chr14:81442892..81444755,2	MCF-7	breast:
27	chr14:81420793..81423189-chr14:81424553..81427836,4	MCF-7	breast:
28	chr14:81401790..81404001-chr14:81408260..81409826,2	K562	blood:
29	chr14:81447196..81448849-chr14:81635444..81638287,2	MCF-7	breast:
30	chr14:81421307..81423560-chr14:81685821..81687772,2	MCF-7	breast:
31	chr14:81401790..81404001-chr14:81408260..81409826,2	K562	blood:
32	chr14:81429871..81432242-chr14:81433461..81436310,2	MCF-7	breast:
33	chr14:81432696..81434242-chr14:81439337..81441996,2	MCF-7	breast:
34	chr14:81405070..81407655-chr14:81893214..81894963,2	K562	blood:
35	chr14:81427260..81428823-chr14:81430386..81432233,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP128-1	chr14:81411900-81412111	NONHSAT038042
2	lnc-CEP128-1	chr14:81425776-81425850	NONHSAT038045
3	lnc-NRXN3-4	chr14:81448332-81449982	NONHSAT038046
4	lnc-CEP128-1	chr14:81425776-81425861	NONHSAT038042
5	lnc-CEP128-1	chr14:81424522-81424629	NONHSAT038042
6	lnc-CEP128-1	chr14:81424142-81424629	NONHSAT038045

No data

Variant related genes	Relation type
TSHR	TF binding region
CEP128	TF binding region
ENSG00000258915	TF binding region
TSHR	CpG island
CEP128	CpG island
ENSG00000258915	CpG island
ENSG00000258915	chromatin interactions
ENSG00000258999	chromatin interactions
ENSG00000165409	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000100629	chromatin interactions
ENSG00000140022	chromatin interactions

Extended variants
information (count: 1768 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1768 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2195101	chr14:81399692-81399693	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574917409	chr14:81399714-81399715	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2195102	chr14:81399718-81399719	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs187465545	chr14:81399727-81399728	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117165970	chr14:81399796-81399797	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540101819	chr14:81399864-81399865	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367557483	chr14:81399871-81399872	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149426059	chr14:81399939-81399940	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560538997	chr14:81400029-81400030	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2217176	chr14:81400050-81400051	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs550872031	chr14:81400066-81400067	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562742766	chr14:81400087-81400088	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72693043	chr14:81400093-81400094	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs370753862	chr14:81400141-81400142	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551711284	chr14:81400162-81400163	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566853110	chr14:81400225-81400226	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534293595	chr14:81400236-81400237	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs192012398	chr14:81400250-81400251	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369385687	chr14:81400252-81400253	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540370884	chr14:81400262-81400263	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371805558	chr14:81400267-81400268	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143671294	chr14:81400281-81400282	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112410969	chr14:81400304-81400305	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556456539	chr14:81400324-81400325	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577879079	chr14:81400363-81400364	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189310582	chr14:81400391-81400392	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs386779253	chr14:81400425-81400426	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12878167	chr14:81400427-81400428	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs540308092	chr14:81400470-81400471	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550433193	chr14:81400519-81400520	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561893799	chr14:81400541-81400542	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs116855873	chr14:81400561-81400562	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73344075	chr14:81400564-81400565	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs148086023	chr14:81400576-81400577	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142894006	chr14:81400654-81400655	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545116842	chr14:81400671-81400672	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs117128935	chr14:81400698-81400699	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146079296	chr14:81400741-81400742	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117465362	chr14:81400748-81400749	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116952580	chr14:81400751-81400752	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs9323695	chr14:81400766-81400767	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs115373828	chr14:81400776-81400777	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139329694	chr14:81400781-81400782	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539310330	chr14:81400793-81400794	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557504802	chr14:81400803-81400804	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566442804	chr14:81400825-81400826	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs193294936	chr14:81400903-81400904	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537582419	chr14:81400916-81400917	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533525376	chr14:81400970-81400971	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142526708	chr14:81400975-81400976	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81359400-81406000	Weak transcription	A549	lung
2	chr14:81359800-81407200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:81375400-81407600	Weak transcription	Gastric	stomach
4	chr14:81379400-81407400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr14:81382600-81406400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr14:81387800-81407200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:81390000-81405000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr14:81390000-81407200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr14:81392200-81407200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr14:81392400-81406600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr14:81392600-81407200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr14:81392600-81407200	Weak transcription	Fetal Stomach	stomach
13	chr14:81392800-81407400	Weak transcription	Esophagus	oesophagus
14	chr14:81393000-81407600	Weak transcription	Lung	lung
15	chr14:81393600-81407200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr14:81394000-81407400	Weak transcription	Left Ventricle	heart
17	chr14:81395000-81407400	Weak transcription	Fetal Intestine Large	intestine
18	chr14:81396000-81399800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:81396000-81401000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr14:81396400-81407600	Weak transcription	Aorta	Aorta
21	chr14:81397400-81407200	Weak transcription	Ovary	ovary
22	chr14:81397600-81400000	Enhancers	Primary hematopoietic stem cells	blood
23	chr14:81397800-81400600	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr14:81398000-81400600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:81398000-81407200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:81398000-81407200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr14:81398000-81407200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr14:81398200-81399800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr14:81398200-81406600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr14:81398200-81407000	Weak transcription	Primary T cells from cord blood	blood
31	chr14:81398200-81407200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr14:81398200-81407400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:81398400-81400000	Enhancers	K562	blood
34	chr14:81398400-81406000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr14:81398400-81406800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr14:81398600-81400800	Strong transcription	Fetal Thymus	thymus
37	chr14:81398600-81406400	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr14:81398800-81406200	Genic enhancers	Dnd41	blood
39	chr14:81398800-81406600	Weak transcription	HMEC	breast
40	chr14:81398800-81407200	Weak transcription	Primary B cells from cord blood	blood
41	chr14:81399000-81399800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr14:81399000-81400200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:81399000-81402400	Weak transcription	NHEK	skin
44	chr14:81399000-81406400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr14:81399000-81406400	Weak transcription	GM12878-XiMat	blood
46	chr14:81399200-81400200	Enhancers	HSMMtube	muscle
47	chr14:81399200-81400600	Strong transcription	Thymus	Thymus
48	chr14:81399400-81399800	Enhancers	Spleen	Spleen
49	chr14:81399400-81400800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:81399400-81400800	Enhancers	Brain Germinal Matrix	brain

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