Variant report

Variant	nsv534143
Chromosome Location	chr14:36747497-36787893
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	chr14:36786874-36787050	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:36754429-36754629	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:36784635-36784815	K562	blood:	n/a	n/a
4	ARID3A	chr14:36785526-36785702	K562	blood:	n/a	n/a
5	ARID3A	chr14:36754518-36754696	K562	blood:	n/a	n/a
6	ARID3A	chr14:36769601-36770046	HepG2	liver:	n/a	n/a
7	ATF2	chr14:36769592-36769971	GM12878	blood:	n/a	n/a
8	ATF2	chr14:36769598-36769998	GM12878	blood:	n/a	n/a
9	BACH1	chr14:36764628-36764681	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr14:36784705-36785059	GM12878	blood:	n/a	chr14:36784842-36784853
11	BATF	chr14:36769541-36769888	GM12878	blood:	n/a	chr14:36769803-36769813
12	BATF	chr14:36784726-36785054	GM12878	blood:	n/a	chr14:36784842-36784853
13	BCL11A	chr14:36769496-36769723	GM12878	blood:	n/a	n/a
14	BCL3	chr14:36784682-36784987	GM12878	blood:	n/a	chr14:36784811-36784820
15	BHLHE40	chr14:36784748-36785137	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:36754810-36755151	K562	blood:	n/a	n/a
17	CBX3	chr14:36750501-36750838	K562	blood:	n/a	n/a
18	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
19	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
20	CEBPB	chr14:36763101-36763325	Hela-S3	cervix:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
21	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
22	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
23	CEBPB	chr14:36785526-36785655	K562	blood:	n/a	n/a
24	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
25	CEBPB	chr14:36766524-36766696	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:36778595-36778871	HepG2	liver:	n/a	chr14:36778710-36778718 chr14:36778717-36778728 chr14:36778716-36778729 chr14:36778716-36778727
27	CEBPB	chr14:36766487-36766790	A549	lung:	n/a	n/a
28	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
29	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
30	CEBPB	chr14:36769071-36769262	K562	blood:	n/a	chr14:36769203-36769214
31	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
32	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
33	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
34	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
35	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
36	CEBPB	chr14:36766523-36766538	K562	blood:	n/a	n/a
37	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
38	CEBPB	chr14:36763112-36763367	A549	lung:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
39	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
40	CEBPB	chr14:36769079-36769350	HepG2	liver:	n/a	chr14:36769203-36769214
41	CEBPB	chr14:36763024-36763394	IMR90	lung:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
42	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
43	CEBPB	chr14:36763053-36763383	HepG2	liver:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
44	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
45	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
46	CEBPB	chr14:36766487-36766828	HepG2	liver:	n/a	n/a
47	CEBPD	chr14:36754201-36754816	K562	blood:	n/a	chr14:36754380-36754391 chr14:36754381-36754390 chr14:36754380-36754391
48	CHD2	chr14:36773241-36773404	K562	blood:	n/a	n/a
49	CHD2	chr14:36750581-36750860	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr14:36784620-36785008	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36783435-36783485	HCPEpiC	choroid plexus:	n/a
2	chr14:36783435-36783485	HCPEpiC	choroid plexus:	n/a
3	chr14:36765887-36765937	Jurkat	blood:	n/a
4	chr14:36765887-36765937	Hepatocyte	liver:	n/a
5	chr14:36765887-36765937	HMEC	breast:	n/a
6	chr14:36783435-36783485	HIPEpiC	eye:	n/a
7	chr14:36783435-36783485	AG04450	lung:	fetal
8	chr14:36765887-36765937	AG04450	lung:	fetal
9	chr14:36783435-36783485	HCT-116	colon:	n/a
10	chr14:36765887-36765937	CMK	blood:	n/a
11	chr14:36765887-36765937	AG10803	skin:	n/a
12	chr14:36765887-36765937	NT2-D1	testis:	n/a
13	chr14:36783435-36783485	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:36783435-36783485	AoSMC	blood vessel:	n/a
15	chr14:36783435-36783485	PANC-1	pancreas:	n/a
16	chr14:36765887-36765937	Caco-2	colon:	n/a
17	chr14:36765887-36765937	GM06990	blood:	n/a
18	chr14:36765887-36765937	ovcar-3	ovarian:	n/a
19	chr14:36765887-36765937	GM12892	blood:	n/a
20	chr14:36765887-36765937	SAEC	small airway:	n/a
21	chr14:36783435-36783485	HEEpiC	esophagus:	n/a
22	chr14:36765887-36765937	PANC-1	pancreas:	n/a
23	chr14:36783435-36783485	HRE	kidney:	n/a
24	chr14:36783435-36783485	AG09319	gingival:	n/a
25	chr14:36783435-36783485	GM12892	blood:	n/a
26	chr14:36765887-36765937	AG04449	skin:	fetal
27	chr14:36765887-36765937	SK-N-SH_RA	brain:	n/a
28	chr14:36783435-36783485	SK-N-SH_RA	brain:	n/a
29	chr14:36783435-36783485	Caco-2	colon:	n/a
30	chr14:36783435-36783485	HCF	heart:	n/a
31	chr14:36765887-36765937	Hela-S3	cervix:	n/a
32	chr14:36783435-36783485	LNCaP	prostate:	n/a
33	chr14:36765887-36765937	ProgFib	skin:	n/a
34	chr14:36765887-36765937	SK-N-MC	brain:	n/a
35	chr14:36783435-36783485	PrEC	prostate:	n/a
36	chr14:36765887-36765937	HEK293	kidney:	embryo
37	chr14:36783435-36783485	CMK	blood:	n/a
38	chr14:36765887-36765937	BE2_C	brain:	n/a
39	chr14:36783435-36783485	HNPCEpiC	eye:	n/a
40	chr14:36765887-36765937	HRPEpiC	eye:	n/a
41	chr14:36783435-36783485	GM06990	blood:	n/a
42	chr14:36783435-36783485	IMR90	lung:	fetal
43	chr14:36765887-36765937	HNPCEpiC	eye:	n/a
44	chr14:36783435-36783485	ECC-1	luminal epithelium:	n/a
45	chr14:36783435-36783485	SK-N-SH	brain:	n/a
46	chr14:36765887-36765937	HCT-116	colon:	n/a
47	chr14:36765887-36765937	HIPEpiC	eye:	n/a
48	chr14:36765887-36765937	SKMC	muscle:	n/a
49	chr14:36783435-36783485	MCF10A-Er-Src	breast:	n/a
50	chr14:36783435-36783485	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
2	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
3	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
4	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
5	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
6	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
7	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
8	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
9	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
10	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
11	chr14:36780477..36782487-chr14:36786743..36788959,2	MCF-7	breast:
12	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
13	chr14:36777999..36779910-chr14:36780693..36782263,2	K562	blood:
14	chr14:36744274..36747113-chr14:36751672..36754404,2	K562	blood:
15	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
16	chr14:36539398..36539927-chr14:36782854..36783534,2	MCF-7	breast:
17	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
18	chr1:53308102..53308983-chr14:36776394..36777212,2	MCF-7	breast:
19	chr14:36747753..36750130-chr14:36837234..36840040,2	K562	blood:
20	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
21	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:
22	chr14:36574817..36577069-chr14:36759896..36761522,2	K562	blood:
23	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
24	chr14:36764356..36766660-chr14:36769237..36771689,3	K562	blood:
25	chr14:36762587..36764557-chr14:36781250..36784124,2	MCF-7	breast:
26	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
27	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
28	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
29	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
30	chr14:36777645..36780229-chr14:36786756..36790572,4	MCF-7	breast:
31	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
32	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
33	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
34	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
35	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
36	chr14:36774640..36777657-chr14:36778032..36780826,3	K562	blood:
37	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
38	chr14:36784077..36786059-chr14:36788034..36791140,4	MCF-7	breast:
39	chr14:36778847..36780826-chr14:36784208..36786054,2	MCF-7	breast:
40	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
41	chr14:36774640..36776851-chr14:36779144..36781211,2	K562	blood:
42	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
43	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFTA3-2	chr14:36785664-36785887	uc_374_-
2	lnc-PAX9-10	chr14:36785664-36785887	uc_374_+
3	lnc-BRMS1L-4	chr14:36758889-36759236	XLOC_010799

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

Extended variants
information (count: 1262 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558974796	chr14:36747509-36747510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34723409	chr14:36747533-36747534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534862183	chr14:36747561-36747562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577772599	chr14:36747578-36747579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562025956	chr14:36747603-36747604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540377150	chr14:36747608-36747609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80145612	chr14:36747617-36747618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76289835	chr14:36747618-36747619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61994971	chr14:36747620-36747621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553394085	chr14:36747624-36747625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542681827	chr14:36747639-36747640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562447628	chr14:36747677-36747678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531308489	chr14:36747684-36747685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192333561	chr14:36747751-36747752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184540898	chr14:36747786-36747787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527923741	chr14:36747851-36747852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189828736	chr14:36747866-36747867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137855430	chr14:36747893-36747894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536525337	chr14:36747917-36747918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141121014	chr14:36747922-36747923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569730106	chr14:36747974-36747975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs17104271	chr14:36747977-36747978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs558786690	chr14:36748010-36748011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542155562	chr14:36748089-36748090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542664645	chr14:36748123-36748124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192942635	chr14:36748131-36748132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533789014	chr14:36748138-36748139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553918890	chr14:36748167-36748168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574014377	chr14:36748268-36748269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116138940	chr14:36748295-36748296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35330290	chr14:36748319-36748320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184627474	chr14:36748387-36748388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576107480	chr14:36748504-36748505	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs8018390	chr14:36748541-36748542	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs564869417	chr14:36748573-36748574	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs527362761	chr14:36748625-36748626	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575692156	chr14:36748668-36748669	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs541290745	chr14:36748682-36748683	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs17104274	chr14:36748686-36748687	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs530197306	chr14:36748707-36748708	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs546333766	chr14:36748775-36748776	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs550070200	chr14:36748782-36748783	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs375413847	chr14:36748784-36748785	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs144932266	chr14:36748810-36748811	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs148267995	chr14:36748844-36748845	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs372098708	chr14:36748880-36748881	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566077422	chr14:36748930-36748931	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs533710341	chr14:36748936-36748937	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs141280499	chr14:36748944-36748945	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs189555848	chr14:36748963-36748964	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	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
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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr14:36745400-36748200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr14:36745400-36748200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr14:36745400-36748400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr14:36745400-36748400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr14:36745600-36748200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr14:36745600-36750600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:36745800-36748800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr14:36746400-36748400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:36746600-36748600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:36747000-36748400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr14:36747000-36748400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr14:36747600-36748000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr14:36748000-36748400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:36748200-36749000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:36748200-36749400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:36748200-36750200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr14:36748200-36751000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr14:36748400-36748600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr14:36748400-36748600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr14:36748400-36748800	Active TSS	Brain Hippocampus Middle	brain
25	chr14:36748400-36748800	Bivalent Enhancer	Fetal Brain Female	brain
26	chr14:36748400-36749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr14:36748400-36749000	Active TSS	Brain Anterior Caudate	brain
28	chr14:36748400-36749200	Active TSS	Brain Cingulate Gyrus	brain
29	chr14:36748400-36749400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr14:36748400-36749400	Enhancers	Brain Substantia Nigra	brain
31	chr14:36748400-36749600	Enhancers	Brain Germinal Matrix	brain
32	chr14:36748400-36749800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr14:36748400-36750600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:36748400-36750600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr14:36748400-36751000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr14:36748600-36748800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr14:36748600-36749000	Enhancers	NHEK	skin
38	chr14:36748600-36749400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr14:36748600-36749400	Enhancers	HMEC	breast
40	chr14:36748600-36749600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr14:36748600-36749800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr14:36748600-36749800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:36748600-36750400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:36748800-36749000	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr14:36748800-36749000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr14:36748800-36749000	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr14:36748800-36749200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr14:36748800-36749400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr14:36749000-36749200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr14:36749000-36749200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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