Variant report

Variant	nsv932413
Chromosome Location	chr10:91294861-91300246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:91295652-91295970	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr10:91295545-91295838	H1-hESC	embryonic stem cell:	n/a	chr10:91295780-91295790 chr10:91295565-91295575
3	CHD2	chr10:91295642-91295914	H1-hESC	embryonic stem cell:	n/a	chr10:91295780-91295790
4	CHD2	chr10:91296168-91296202	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr10:91295420-91295570	AG04449	skin:	n/a	n/a
6	CTCF	chr10:91295360-91295510	AoAF	blood vessel:	n/a	chr10:91295409-91295422
7	CTCF	chr10:91295382-91295555	H1-hESC	embryonic stem cell:	n/a	chr10:91295409-91295422
8	CTCF	chr10:91295380-91295530	SK-N-SH_RA	brain:	n/a	chr10:91295409-91295422
9	CTCF	chr10:91295300-91295450	GM12871	blood:	n/a	chr10:91295409-91295422
10	CTCF	chr10:91295454-91295500	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr10:91295380-91295530	GM12868	blood:	n/a	chr10:91295409-91295422
12	CTCF	chr10:91295440-91295590	AG09319	gingival:	n/a	n/a
13	CTCF	chr10:91295400-91295550	WERI-Rb-1	eye:	n/a	chr10:91295409-91295422
14	CTCF	chr10:91295380-91295530	HEK293	kidney:	n/a	chr10:91295409-91295422
15	CTCF	chr10:91295420-91295570	HepG2	liver:	n/a	n/a
16	CTCF	chr10:91295640-91295790	SAEC	small airway:	n/a	n/a
17	CTCF	chr10:91295320-91295470	AoAF	blood vessel:	n/a	chr10:91295409-91295422
18	CTCF	chr10:91295360-91295510	AG04449	skin:	n/a	chr10:91295409-91295422
19	CTCF	chr10:91295360-91295510	HRPEpiC	eye:	n/a	chr10:91295409-91295422
20	CTCF	chr10:91295400-91295550	GM12867	blood:	n/a	chr10:91295409-91295422
21	CTCF	chr10:91295420-91295570	HEK293	kidney:	n/a	n/a
22	CTCF	chr10:91295300-91295450	HCM	heart:	n/a	chr10:91295409-91295422
23	CTCF	chr10:91295440-91295590	GM12866	blood:	n/a	n/a
24	CTCF	chr10:91295422-91295578	IMR90	lung:	n/a	n/a
25	CTCF	chr10:91295360-91295510	HBMEC	blood vessel:	n/a	chr10:91295409-91295422
26	CTCF	chr10:91295440-91295590	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr10:91295440-91295590	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr10:91295400-91295550	HAc	cerebellar:	n/a	chr10:91295409-91295422
29	CTCF	chr10:91295340-91295490	GM12875	blood:	n/a	chr10:91295409-91295422
30	CTCF	chr10:91295420-91295570	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr10:91295600-91295750	HCM	heart:	n/a	n/a
32	CTCF	chr10:91295003-91295034	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:91295580-91295730	HRPEpiC	eye:	n/a	n/a
34	E2F6	chr10:91294820-91295955	H1-hESC	embryonic stem cell:	n/a	chr10:91295386-91295395 chr10:91295424-91295433
35	E2F6	chr10:91294894-91295390	A549	lung:	n/a	n/a
36	E2F6	chr10:91294689-91295989	H1-hESC	embryonic stem cell:	n/a	chr10:91295386-91295395 chr10:91295424-91295433
37	EP300	chr10:91295402-91295690	H1-hESC	embryonic stem cell:	n/a	chr10:91295416-91295432
38	EP300	chr10:91300209-91300599	SK-N-SH_RA	brain:	n/a	n/a
39	FOSL2	chr10:91300161-91300807	SK-N-SH	brain:	n/a	chr10:91300526-91300534 chr10:91300526-91300533
40	GABPA	chr10:91295411-91295872	H1-hESC	embryonic stem cell:	n/a	n/a
41	GATA3	chr10:91300193-91300730	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr10:91300089-91300757	SK-N-SH	brain:	n/a	n/a
43	GTF2F1	chr10:91295998-91296130	H1-hESC	embryonic stem cell:	n/a	n/a
44	GTF2F1	chr10:91295136-91295240	H1-hESC	embryonic stem cell:	n/a	n/a
45	GTF2F1	chr10:91295564-91295781	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr10:91300202-91300815	SK-N-SH	brain:	n/a	chr10:91300526-91300534 chr10:91300526-91300533
47	JUND	chr10:91295489-91295668	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAX	chr10:91294695-91295373	A549	lung:	n/a	chr10:91295016-91295026 chr10:91295015-91295026 chr10:91295015-91295026 chr10:91295015-91295026
49	MAX	chr10:91294812-91295235	A549	lung:	n/a	chr10:91295016-91295026 chr10:91295015-91295026 chr10:91295015-91295026 chr10:91295015-91295026
50	MAX	chr10:91294829-91295606	H1-hESC	embryonic stem cell:	n/a	chr10:91295016-91295026 chr10:91295015-91295026 chr10:91295015-91295026 chr10:91295015-91295026 chr10:91295425-91295435

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91295159-91295209	T-47D	breast:	n/a
2	chr10:91295159-91295209	T-47D	breast:	n/a
3	chr10:91295650-91295700	HRE	kidney:	n/a
4	chr10:91294839-91294889	PFSK-1	brain:	n/a
5	chr10:91295338-91295388	AG04449	skin:	fetal
6	chr10:91295855-91295905	GM19239	blood:	n/a
7	chr10:91295650-91295700	HNPCEpiC	eye:	n/a
8	chr10:91295045-91295095	Hela-S3	cervix:	n/a
9	chr10:91295855-91295905	SKMC	muscle:	n/a
10	chr10:91296252-91296302	SK-N-MC	brain:	n/a
11	chr10:91296252-91296302	GM06990	blood:	n/a
12	chr10:91295358-91295408	CMK	blood:	n/a
13	chr10:91295045-91295095	BE2_C	brain:	n/a
14	chr10:91295650-91295700	Hela-S3	cervix:	n/a
15	chr10:91295317-91295367	HCPEpiC	choroid plexus:	n/a
16	chr10:91295421-91295471	HRPEpiC	eye:	n/a
17	chr10:91295643-91295693	GM12878	blood:	n/a
18	chr10:91296252-91296302	PrEC	prostate:	n/a
19	chr10:91295045-91295095	LNCaP	prostate:	n/a
20	chr10:91296252-91296302	HRE	kidney:	n/a
21	chr10:91296252-91296302	H1-hESC	embryonic stem cell:	embryo
22	chr10:91295643-91295693	MCF10A-Er-Src	breast:	n/a
23	chr10:91295650-91295700	K562	blood:	n/a
24	chr10:91296457-91296507	Hepatocyte	liver:	n/a
25	chr10:91294839-91294889	T-47D	breast:	n/a
26	chr10:91295159-91295209	HIPEpiC	eye:	n/a
27	chr10:91295410-91295460	AG09319	gingival:	n/a
28	chr10:91295159-91295209	HCF	heart:	n/a
29	chr10:91296311-91296361	Hepatocyte	liver:	n/a
30	chr10:91295650-91295700	MCF10A-Er-Src	breast:	n/a
31	chr10:91295299-91295349	ovcar-3	ovarian:	n/a
32	chr10:91295159-91295209	Hepatocyte	liver:	n/a
33	chr10:91295338-91295388	K562	blood:	n/a
34	chr10:91296457-91296507	GM12892	blood:	n/a
35	chr10:91295317-91295367	AG04449	skin:	fetal
36	chr10:91295421-91295471	PFSK-1	brain:	n/a
37	chr10:91295159-91295209	HL-60	blood:	n/a
38	chr10:91295045-91295095	PrEC	prostate:	n/a
39	chr10:91295650-91295700	HL-60	blood:	n/a
40	chr10:91296457-91296507	HUVEC	blood vessel:	n/a
41	chr10:91294839-91294889	SKMC	muscle:	n/a
42	chr10:91295317-91295367	SKMC	muscle:	n/a
43	chr10:91295643-91295693	SK-N-SH_RA	brain:	n/a
44	chr10:91295410-91295460	HRPEpiC	eye:	n/a
45	chr10:91296252-91296302	HCM	heart:	n/a
46	chr10:91295346-91295396	GM12892	blood:	n/a
47	chr10:91295159-91295209	NHDF-neo	bronchial:	n/a
48	chr10:91295358-91295408	NHBE	bronchial:	n/a
49	chr10:91295045-91295095	T-47D	breast:	n/a
50	chr10:91295421-91295471	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:91289979..91292393-chr10:91298725..91300653,2	K562	blood:

Variant related genes	Relation type
SLC16A12	TF binding region
SLC16A12	CpG island

Extended variants
information (count: 224 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:224 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193142267	chr10:91294952-91294953	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73363824	chr10:91294974-91294975	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs113441321	chr10:91295021-91295022	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557712602	chr10:91295050-91295051	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577642900	chr10:91295121-91295122	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570166460	chr10:91295148-91295149	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553863777	chr10:91295168-91295169	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574110132	chr10:91295171-91295172	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543203249	chr10:91295204-91295205	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369443089	chr10:91295223-91295224	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562980966	chr10:91295253-91295254	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377006943	chr10:91295337-91295338	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs545406223	chr10:91295380-91295381	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs184932556	chr10:91295400-91295401	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs189781717	chr10:91295401-91295402	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs546680974	chr10:91295431-91295432	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs560294763	chr10:91295497-91295498	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529023523	chr10:91295543-91295544	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs549149516	chr10:91295566-91295567	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs71022572	chr10:91295603-91295604	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs398014396	chr10:91295607-91295608	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs180982909	chr10:91295674-91295675	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs77951812	chr10:91295685-91295686	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs538120164	chr10:91295786-91295787	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs551283145	chr10:91295815-91295816	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs141898054	chr10:91295833-91295834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370211657	chr10:91295835-91295836	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571271416	chr10:91295843-91295844	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs533941681	chr10:91295873-91295874	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs373905598	chr10:91295914-91295915	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs111792021	chr10:91295917-91295918	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs111820712	chr10:91295918-91295919	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs553802342	chr10:91295982-91295983	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs574070708	chr10:91295988-91295989	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs536381338	chr10:91296012-91296013	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs556697064	chr10:91296100-91296101	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs576584718	chr10:91296112-91296113	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs73363825	chr10:91296117-91296118	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565589024	chr10:91296149-91296150	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs144751149	chr10:91296197-91296198	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs77097927	chr10:91296204-91296205	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs560228203	chr10:91296251-91296252	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs72816757	chr10:91296362-91296363	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs545885854	chr10:91296372-91296373	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs74370355	chr10:91296375-91296376	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs562673819	chr10:91296457-91296458	Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs531421820	chr10:91296477-91296478	Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs537127258	chr10:91296491-91296492	Bivalent Enhancer Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs563697179	chr10:91296557-91296558	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571210811	chr10:91296560-91296561	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91293200-91296000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
2	chr10:91293600-91295000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
3	chr10:91293600-91295000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
4	chr10:91293800-91295400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
5	chr10:91293800-91295800	Active TSS	H9 Cell Line	embryonic stem cell
6	chr10:91293800-91295800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
7	chr10:91293800-91296000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr10:91293800-91296200	Active TSS	Pancreas	Pancrea
9	chr10:91294000-91295000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr10:91294000-91295000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
11	chr10:91294000-91295000	Bivalent Enhancer	HUVEC	blood vessel
12	chr10:91294000-91296000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr10:91294000-91296000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
14	chr10:91294000-91296000	Weak transcription	Fetal Heart	heart
15	chr10:91294000-91296000	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr10:91294000-91296200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr10:91294200-91295200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:91294200-91295200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr10:91294200-91295800	Active TSS	Left Ventricle	heart
20	chr10:91294200-91295800	Bivalent/Poised TSS	Psoas Muscle	Psoas
21	chr10:91294200-91295800	Active TSS	Right Ventricle	heart
22	chr10:91294400-91295000	Enhancers	Liver	Liver
23	chr10:91294400-91295200	Active TSS	Fetal Kidney	kidney
24	chr10:91294400-91295400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
25	chr10:91294400-91295400	Flanking Bivalent TSS/Enh	Placenta	Placenta
26	chr10:91294400-91295800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr10:91294400-91295800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
28	chr10:91294400-91295800	Bivalent/Poised TSS	A549	lung
29	chr10:91294400-91295800	Bivalent/Poised TSS	NH-A	brain
30	chr10:91294600-91295000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr10:91294600-91295000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr10:91294600-91295000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
33	chr10:91294600-91295000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
34	chr10:91294600-91295200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
35	chr10:91294600-91295200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr10:91294600-91295200	Bivalent Enhancer	Brain Angular Gyrus	brain
37	chr10:91294600-91295200	Bivalent Enhancer	Fetal Brain Male	brain
38	chr10:91294600-91295600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
39	chr10:91294600-91295800	Bivalent Enhancer	Fetal Thymus	thymus
40	chr10:91294600-91296000	Bivalent/Poised TSS	Fetal Brain Female	brain
41	chr10:91294600-91296000	Active TSS	Right Atrium	heart
42	chr10:91294800-91295000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr10:91294800-91295000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:91294800-91295000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr10:91294800-91295000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:91294800-91295000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr10:91294800-91295000	Bivalent Enhancer	Brain Anterior Caudate	brain
48	chr10:91294800-91295000	Bivalent Enhancer	Brain Substantia Nigra	brain
49	chr10:91294800-91295000	Bivalent Enhancer	Fetal Intestine Large	intestine
50	chr10:91294800-91295000	Active TSS	Ovary	ovary

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