Variant report

Variant	esv2751271
Chromosome Location	chr14:36745649-36782949
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	ARID3A	chr14:36754518-36754696	K562	blood:	n/a	n/a
2	ARID3A	chr14:36769601-36770046	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:36754429-36754629	HepG2	liver:	n/a	n/a
4	ATF2	chr14:36769592-36769971	GM12878	blood:	n/a	n/a
5	ATF2	chr14:36769598-36769998	GM12878	blood:	n/a	n/a
6	BACH1	chr14:36764628-36764681	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:36769541-36769888	GM12878	blood:	n/a	chr14:36769803-36769813
8	BCL11A	chr14:36769496-36769723	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:36754810-36755151	K562	blood:	n/a	n/a
10	CBX3	chr14:36750501-36750838	K562	blood:	n/a	n/a
11	CEBPB	chr14:36754191-36754568	A549	lung:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
12	CEBPB	chr14:36766487-36766828	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:36754258-36754482	HepG2	liver:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
14	CEBPB	chr14:36754191-36754575	IMR90	lung:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
15	CEBPB	chr14:36763053-36763383	HepG2	liver:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
16	CEBPB	chr14:36754102-36754663	K562	blood:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
17	CEBPB	chr14:36754195-36754553	HepG2	liver:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
18	CEBPB	chr14:36763101-36763325	Hela-S3	cervix:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
19	CEBPB	chr14:36766487-36766790	A549	lung:	n/a	n/a
20	CEBPB	chr14:36754106-36754663	MCF-7	breast:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
21	CEBPB	chr14:36769071-36769262	K562	blood:	n/a	chr14:36769203-36769214
22	CEBPB	chr14:36766523-36766538	K562	blood:	n/a	n/a
23	CEBPB	chr14:36754112-36754592	A549	lung:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
24	CEBPB	chr14:36754235-36754547	K562	blood:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
25	CEBPB	chr14:36754153-36754579	A549	lung:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
26	CEBPB	chr14:36769079-36769350	HepG2	liver:	n/a	chr14:36769203-36769214
27	CEBPB	chr14:36754149-36754579	ECC-1	luminal epithelium:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
28	CEBPB	chr14:36763024-36763394	IMR90	lung:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
29	CEBPB	chr14:36763112-36763367	A549	lung:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
30	CEBPB	chr14:36754119-36754606	K562	blood:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
31	CEBPB	chr14:36754194-36754566	H1-hESC	embryonic stem cell:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
32	CEBPB	chr14:36766524-36766696	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:36754236-36754520	HepG2	liver:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
34	CEBPB	chr14:36754202-36754578	Hela-S3	cervix:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
35	CEBPB	chr14:36754192-36754580	HepG2	liver:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
36	CEBPB	chr14:36754155-36754602	ECC-1	luminal epithelium:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
37	CEBPB	chr14:36754157-36754577	MCF-7	breast:	n/a	chr14:36754379-36754392 chr14:36754379-36754390 chr14:36754381-36754390 chr14:36754381-36754390 chr14:36754379-36754392 chr14:36754381-36754390 chr14:36754381-36754390
38	CEBPB	chr14:36778595-36778871	HepG2	liver:	n/a	chr14:36778710-36778718 chr14:36778717-36778728 chr14:36778716-36778729 chr14:36778716-36778727
39	CEBPD	chr14:36754201-36754816	K562	blood:	n/a	chr14:36754380-36754391 chr14:36754381-36754390 chr14:36754380-36754391
40	CHD2	chr14:36773241-36773404	K562	blood:	n/a	n/a
41	CHD2	chr14:36750581-36750860	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr14:36750448-36750888	HepG2	liver:	n/a	n/a
43	CREB1	chr14:36750422-36750914	HepG2	liver:	n/a	n/a
44	CTCF	chr14:36756674-36756728	GM12878	blood:	n/a	n/a
45	CTCF	chr14:36757140-36757290	HepG2	liver:	n/a	n/a
46	CTCF	chr14:36775727-36775789	GM13976	blood:	n/a	n/a
47	CTCF	chr14:36750640-36750790	HepG2	liver:	n/a	n/a
48	CUX1	chr14:36755079-36755154	K562	blood:	n/a	n/a
49	CUX1	chr14:36770982-36771016	GM12878	blood:	n/a	n/a
50	EBF1	chr14:36767540-36767737	GM12878	blood:	n/a	chr14:36767612-36767623

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36765887-36765937	T-47D	breast:	n/a
2	chr14:36765887-36765937	SK-N-SH_RA	brain:	n/a
3	chr14:36765887-36765937	ECC-1	luminal epithelium:	n/a
4	chr14:36765887-36765937	GM19239	blood:	n/a
5	chr14:36765887-36765937	PANC-1	pancreas:	n/a
6	chr14:36765887-36765937	HEK293	kidney:	embryo
7	chr14:36765887-36765937	IMR90	lung:	fetal
8	chr14:36765887-36765937	HIPEpiC	eye:	n/a
9	chr14:36765887-36765937	GM06990	blood:	n/a
10	chr14:36765887-36765937	CMK	blood:	n/a
11	chr14:36765887-36765937	LNCaP	prostate:	n/a
12	chr14:36765887-36765937	PrEC	prostate:	n/a
13	chr14:36765887-36765937	MCF-7	breast:	n/a
14	chr14:36765887-36765937	RPTEC	kidney:	n/a
15	chr14:36765887-36765937	HepG2	liver:	n/a
16	chr14:36765887-36765937	GM12878	blood:	n/a
17	chr14:36765887-36765937	HUVEC	blood vessel:	n/a
18	chr14:36765887-36765937	BJ	skin:	n/a
19	chr14:36765887-36765937	GM12892	blood:	n/a
20	chr14:36765887-36765937	A549	lung:	n/a
21	chr14:36765887-36765937	GM12891	blood:	n/a
22	chr14:36765887-36765937	NT2-D1	testis:	n/a
23	chr14:36765887-36765937	AG04449	skin:	fetal
24	chr14:36765887-36765937	HRE	kidney:	n/a
25	chr14:36765887-36765937	SKMC	muscle:	n/a
26	chr14:36765887-36765937	HL-60	blood:	n/a
27	chr14:36765887-36765937	AG04450	lung:	fetal
28	chr14:36765887-36765937	HEEpiC	esophagus:	n/a
29	chr14:36765887-36765937	HMEC	breast:	n/a
30	chr14:36765887-36765937	HCPEpiC	choroid plexus:	n/a
31	chr14:36765887-36765937	AG09319	gingival:	n/a
32	chr14:36765887-36765937	NB4	blood:	n/a
33	chr14:36765887-36765937	K562	blood:	n/a
34	chr14:36765887-36765937	ProgFib	skin:	n/a
35	chr14:36765887-36765937	BE2_C	brain:	n/a
36	chr14:36765887-36765937	NHDF-neo	bronchial:	n/a
37	chr14:36765887-36765937	ovcar-3	ovarian:	n/a
38	chr14:36765887-36765937	SK-N-SH	brain:	n/a
39	chr14:36765887-36765937	H1-hESC	embryonic stem cell:	embryo
40	chr14:36765887-36765937	AG10803	skin:	n/a
41	chr14:36765887-36765937	PFSK-1	brain:	n/a
42	chr14:36765887-36765937	NHBE	bronchial:	n/a
43	chr14:36765887-36765937	SAEC	small airway:	n/a
44	chr14:36765887-36765937	HCF	heart:	n/a
45	chr14:36765887-36765937	Hela-S3	cervix:	n/a
46	chr14:36765887-36765937	Caco-2	colon:	n/a
47	chr14:36765887-36765937	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:36765887-36765937	AoSMC	blood vessel:	n/a
49	chr14:36765887-36765937	HNPCEpiC	eye:	n/a
50	chr14:36765887-36765937	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36744274..36747113-chr14:36751672..36754404,2	K562	blood:
2	chr14:36777999..36779910-chr14:36780693..36782263,2	K562	blood:
3	chr14:36574817..36577069-chr14:36759896..36761522,2	K562	blood:
4	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
5	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
6	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
7	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
8	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
9	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
10	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
11	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
12	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
13	chr14:36747753..36750130-chr14:36837234..36840040,2	K562	blood:
14	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
15	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
16	chr14:36739666..36742566-chr14:36744671..36747415,2	K562	blood:
17	chr14:36764356..36766660-chr14:36769237..36771689,3	K562	blood:
18	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
19	chr14:36744274..36747113-chr14:36751672..36754404,2	K562	blood:
20	chr14:36774640..36777657-chr14:36778032..36780826,3	K562	blood:
21	chr14:36777645..36780229-chr14:36786756..36790572,4	MCF-7	breast:
22	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
23	chr1:53308102..53308983-chr14:36776394..36777212,2	MCF-7	breast:
24	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
25	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
26	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
27	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
28	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
29	chr14:36774640..36776851-chr14:36779144..36781211,2	K562	blood:
30	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:
31	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
32	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
33	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
34	chr14:36762587..36764557-chr14:36781250..36784124,2	MCF-7	breast:
35	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
36	chr14:36539398..36539927-chr14:36782854..36783534,2	MCF-7	breast:
37	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
38	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:
39	chr14:36738662..36740717-chr14:36743320..36745881,2	MCF-7	breast:
40	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRMS1L-4	chr14:36747208-36747276	XLOC_010799
2	lnc-BRMS1L-4	chr14:36758889-36759236	XLOC_010799

Variant related genes	Relation type
MBIP	TF binding region
MBIP	CpG island
ENSG00000151332	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000203995	chromatin interactions

Extended variants
information (count: 1168 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3844013	chr14:36745669-36745670	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543996352	chr14:36745713-36745714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564444495	chr14:36745721-36745722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564306899	chr14:36745722-36745723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs202083444	chr14:36745732-36745733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528259875	chr14:36745736-36745737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546936136	chr14:36745740-36745741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546602492	chr14:36745778-36745779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150029721	chr14:36745822-36745823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs3909603	chr14:36745938-36745939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs190626059	chr14:36745939-36745940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568927867	chr14:36745966-36745967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182883593	chr14:36746161-36746162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114988881	chr14:36746207-36746208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377591077	chr14:36746212-36746213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571943938	chr14:36746226-36746227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs5807861	chr14:36746274-36746275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397853514	chr14:36746281-36746282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75822925	chr14:36746334-36746335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554421461	chr14:36746339-36746340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35555964	chr14:36746490-36746491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191469840	chr14:36746535-36746536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145530656	chr14:36746577-36746578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182840364	chr14:36746666-36746667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12882403	chr14:36746682-36746683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576118555	chr14:36746704-36746705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544035064	chr14:36746740-36746741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565503222	chr14:36746794-36746795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12882169	chr14:36746804-36746805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34074217	chr14:36746849-36746850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564104193	chr14:36746874-36746875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533120361	chr14:36746933-36746934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540173515	chr14:36746989-36746990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560354946	chr14:36746997-36746998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534636910	chr14:36747025-36747026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187957012	chr14:36747026-36747027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148840826	chr14:36747032-36747033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192234665	chr14:36747068-36747069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183524961	chr14:36747114-36747115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs8013261	chr14:36747117-36747118	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs571772934	chr14:36747119-36747120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557523381	chr14:36747134-36747135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17104270	chr14:36747197-36747198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567944153	chr14:36747202-36747203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144855595	chr14:36747238-36747239	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs573831923	chr14:36747325-36747326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536285247	chr14:36747333-36747334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187860796	chr14:36747374-36747375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544655799	chr14:36747385-36747386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576156001	chr14:36747402-36747403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36742400-36753800	Weak transcription	K562	blood
2	chr14:36743000-36748400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:36743800-36747600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:36744200-36757000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:36744800-36746000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:36745200-36745800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr14:36745200-36746400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:36745200-36746400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:36745400-36746200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr14:36745400-36748200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr14:36745400-36748200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr14:36745400-36748400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr14:36745400-36748400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:36745600-36748200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr14:36745600-36750600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr14:36745800-36748800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr14:36746000-36746400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:36746200-36747000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr14:36746400-36746600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr14:36746400-36746800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:36746400-36748400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:36746600-36748600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr14:36746800-36747000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr14:36747000-36748400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr14:36747000-36748400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:36747600-36748000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr14:36748000-36748400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr14:36748200-36749000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr14:36748200-36749400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:36748200-36750200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr14:36748200-36751000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr14:36748400-36748600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr14:36748400-36748600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:36748400-36748800	Active TSS	Brain Hippocampus Middle	brain
35	chr14:36748400-36748800	Bivalent Enhancer	Fetal Brain Female	brain
36	chr14:36748400-36749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr14:36748400-36749000	Active TSS	Brain Anterior Caudate	brain
38	chr14:36748400-36749200	Active TSS	Brain Cingulate Gyrus	brain
39	chr14:36748400-36749400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr14:36748400-36749400	Enhancers	Brain Substantia Nigra	brain
41	chr14:36748400-36749600	Enhancers	Brain Germinal Matrix	brain
42	chr14:36748400-36749800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr14:36748400-36750600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr14:36748400-36750600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr14:36748400-36751000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr14:36748600-36748800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr14:36748600-36749000	Enhancers	NHEK	skin
48	chr14:36748600-36749400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:36748600-36749400	Enhancers	HMEC	breast
50	chr14:36748600-36749600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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