Variant report

Variant	esv34543
Chromosome Location	chr14:36736349-36772564
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	chr14:36769601-36770046	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:36754429-36754629	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:36754518-36754696	K562	blood:	n/a	n/a
4	ARID3A	chr14:36740785-36740980	K562	blood:	n/a	n/a
5	ATF2	chr14:36769598-36769998	GM12878	blood:	n/a	n/a
6	ATF2	chr14:36769592-36769971	GM12878	blood:	n/a	n/a
7	BACH1	chr14:36764628-36764681	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr14:36769541-36769888	GM12878	blood:	n/a	chr14:36769803-36769813
9	BCL11A	chr14:36769496-36769723	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:36754810-36755151	K562	blood:	n/a	n/a
11	CBX3	chr14:36750501-36750838	K562	blood:	n/a	n/a
12	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
13	CEBPB	chr14:36766487-36766828	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:36763112-36763367	A549	lung:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
15	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
16	CEBPB	chr14:36766487-36766790	A549	lung:	n/a	n/a
17	CEBPB	chr14:36769079-36769350	HepG2	liver:	n/a	chr14:36769203-36769214
18	CEBPB	chr14:36738041-36738668	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr14:36763053-36763383	HepG2	liver:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
20	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
21	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
22	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
23	CEBPB	chr14:36769071-36769262	K562	blood:	n/a	chr14:36769203-36769214
24	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
25	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
26	CEBPB	chr14:36745013-36745213	H1-hESC	embryonic stem cell:	n/a	n/a
27	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
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	chr14:36766523-36766538	K562	blood:	n/a	n/a
30	CEBPB	chr14:36766524-36766696	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:36763024-36763394	IMR90	lung:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
32	CEBPB	chr14:36763101-36763325	Hela-S3	cervix:	n/a	chr14:36763198-36763209 chr14:36763198-36763211 chr14:36763199-36763210
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	CEBPD	chr14:36754201-36754816	K562	blood:	n/a	chr14:36754380-36754391 chr14:36754381-36754390 chr14:36754380-36754391
42	CHD2	chr14:36750581-36750860	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr14:36745069-36745264	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr14:36738707-36738907	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr14:36750422-36750914	HepG2	liver:	n/a	n/a
46	CREB1	chr14:36750448-36750888	HepG2	liver:	n/a	n/a
47	CTCF	chr14:36741672-36741750	Fibrobl	skin:	n/a	n/a
48	CTCF	chr14:36743655-36744063	HepG2	liver:	n/a	n/a
49	CTCF	chr14:36743760-36743910	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr14:36743799-36743957	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36743725-36743775	HCM	heart:	n/a
2	chr14:36737696-36737746	GM06990	blood:	n/a
3	chr14:36737696-36737746	NT2-D1	testis:	n/a
4	chr14:36743725-36743775	HRE	kidney:	n/a
5	chr14:36741794-36741844	ovcar-3	ovarian:	n/a
6	chr14:36765887-36765937	BE2_C	brain:	n/a
7	chr14:36741794-36741844	Hela-S3	cervix:	n/a
8	chr14:36765887-36765937	GM12878	blood:	n/a
9	chr14:36743725-36743775	SK-N-SH	brain:	n/a
10	chr14:36741794-36741844	AG10803	skin:	n/a
11	chr14:36741794-36741844	MCF-7	breast:	n/a
12	chr14:36741794-36741844	MCF10A-Er-Src	breast:	n/a
13	chr14:36741645-36741695	SK-N-MC	brain:	n/a
14	chr14:36741794-36741844	BE2_C	brain:	n/a
15	chr14:36765887-36765937	MCF-7	breast:	n/a
16	chr14:36743725-36743775	SK-N-SH_RA	brain:	n/a
17	chr14:36741645-36741695	IMR90	lung:	fetal
18	chr14:36743725-36743775	RPTEC	kidney:	n/a
19	chr14:36737696-36737746	NHDF-neo	bronchial:	n/a
20	chr14:36737696-36737746	SAEC	small airway:	n/a
21	chr14:36743725-36743775	Caco-2	colon:	n/a
22	chr14:36741645-36741695	HNPCEpiC	eye:	n/a
23	chr14:36741794-36741844	HMEC	breast:	n/a
24	chr14:36737696-36737746	HUVEC	blood vessel:	n/a
25	chr14:36737696-36737746	AG09319	gingival:	n/a
26	chr14:36765887-36765937	HCF	heart:	n/a
27	chr14:36741794-36741844	SAEC	small airway:	n/a
28	chr14:36765887-36765937	CMK	blood:	n/a
29	chr14:36743725-36743775	IMR90	lung:	fetal
30	chr14:36765887-36765937	IMR90	lung:	fetal
31	chr14:36741794-36741844	RPTEC	kidney:	n/a
32	chr14:36741645-36741695	GM12891	blood:	n/a
33	chr14:36765887-36765937	NH-A	brain:	n/a
34	chr14:36743725-36743775	LNCaP	prostate:	n/a
35	chr14:36765887-36765937	NHDF-neo	bronchial:	n/a
36	chr14:36737696-36737746	AG04450	lung:	fetal
37	chr14:36737696-36737746	U87	brain:	n/a
38	chr14:36741645-36741695	AG09319	gingival:	n/a
39	chr14:36741794-36741844	Hepatocyte	liver:	n/a
40	chr14:36741645-36741695	HRE	kidney:	n/a
41	chr14:36741645-36741695	LNCaP	prostate:	n/a
42	chr14:36741645-36741695	MCF10A-Er-Src	breast:	n/a
43	chr14:36741645-36741695	A549	lung:	n/a
44	chr14:36741794-36741844	HRPEpiC	eye:	n/a
45	chr14:36743725-36743775	Hepatocyte	liver:	n/a
46	chr14:36743725-36743775	AG10803	skin:	n/a
47	chr14:36741645-36741695	AG09309	skin:	n/a
48	chr14:36741645-36741695	GM12878	blood:	n/a
49	chr14:36743725-36743775	K562	blood:	n/a
50	chr14:36765887-36765937	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36733094..36734657-chr14:36742759..36745467,2	K562	blood:
2	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
3	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
4	chr14:36738662..36740717-chr14:36743320..36745881,2	MCF-7	breast:
5	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
6	chr14:36752607..36756130-chr14:36756602..36759411,3	K562	blood:
7	chr14:36762587..36764557-chr14:36781250..36784124,2	MCF-7	breast:
8	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
9	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
10	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
11	chr14:36764356..36766660-chr14:36769237..36771689,3	K562	blood:
12	chr14:36747753..36750130-chr14:36837234..36840040,2	K562	blood:
13	chr14:36745048..36746882-chr14:36747424..36749342,2	K562	blood:
14	chr14:36733892..36735443-chr14:36737409..36739659,2	K562	blood:
15	chr14:36574817..36577069-chr14:36759896..36761522,2	K562	blood:
16	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
17	chr14:36739666..36742566-chr14:36744671..36747415,2	K562	blood:
18	chr10:69141438..69142223-chr14:36735859..36736731,2	MCF-7	breast:
19	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
20	chr14:36733892..36736595-chr14:36737409..36740158,4	K562	blood:
21	chr14:36744274..36747113-chr14:36751672..36754404,2	K562	blood:
22	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
23	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
24	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
25	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
26	chr14:36744274..36747113-chr14:36751672..36754404,2	K562	blood:
27	chr14:36739666..36742566-chr14:36744671..36747415,2	K562	blood:
28	chr14:36747888..36750635-chr14:36759343..36761098,2	K562	blood:
29	chr14:36733892..36736595-chr14:36737409..36740158,4	K562	blood:
30	chr14:36759414..36761344-chr14:36764422..36766950,2	MCF-7	breast:
31	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
32	chr14:36750490..36753269-chr14:36756385..36758922,2	K562	blood:
33	chr14:36744274..36747863-chr14:36750773..36754664,4	K562	blood:
34	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:
35	chr14:36738662..36740717-chr14:36743320..36745881,2	MCF-7	breast:
36	chr14:36744330..36746505-chr14:36753051..36754941,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRMS1L-4	chr14:36747208-36747276	XLOC_010799
2	lnc-MBIP-1	chr14:36741625-36742658	XLOC_010997
3	lnc-BRMS1L-4	chr14:36741574-36742599	XLOC_010799
4	lnc-BRMS1L-4	chr14:36758889-36759236	XLOC_010799
5	lnc-MBIP-1	chr14:36738278-36738517	XLOC_010997

Variant related genes	Relation type
MBIP	TF binding region
MBIP	CpG island
ENSG00000151332	chromatin interactions
SNAI2	miRNA target sites

Extended variants
information (count: 1143 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1143 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77963087	chr14:36736394-36736395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191183150	chr14:36736449-36736450	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs185726485	chr14:36736451-36736452	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs141668057	chr14:36736456-36736457	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs568515460	chr14:36736462-36736463	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs558877498	chr14:36736470-36736471	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs541886395	chr14:36736504-36736505	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs112306705	chr14:36736689-36736690	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190636683	chr14:36736755-36736756	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150088826	chr14:36736781-36736782	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564773189	chr14:36736790-36736791	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181932760	chr14:36736804-36736805	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540671684	chr14:36736805-36736806	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560526006	chr14:36736819-36736820	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529398202	chr14:36736840-36736841	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549480621	chr14:36736852-36736853	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149242522	chr14:36736923-36736924	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10220683	chr14:36736952-36736953	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566607697	chr14:36736968-36736969	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111663425	chr14:36737007-36737008	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539331521	chr14:36737039-36737040	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576930489	chr14:36737072-36737073	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546216703	chr14:36737112-36737113	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566483523	chr14:36737125-36737126	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535070736	chr14:36737131-36737132	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547204809	chr14:36737142-36737143	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138107519	chr14:36737156-36737157	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142595433	chr14:36737181-36737182	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538488998	chr14:36737270-36737271	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185330120	chr14:36737283-36737284	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578259316	chr14:36737342-36737343	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540908475	chr14:36737346-36737347	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560597156	chr14:36737350-36737351	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573996848	chr14:36737354-36737355	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542607626	chr14:36737393-36737394	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563043702	chr14:36737403-36737404	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531680648	chr14:36737495-36737496	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553112226	chr14:36737516-36737517	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369224606	chr14:36737559-36737560	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550392760	chr14:36737592-36737593	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372680122	chr14:36737605-36737606	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563917873	chr14:36737652-36737653	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532933066	chr14:36737697-36737698	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546504664	chr14:36737742-36737743	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs59879322	chr14:36737750-36737751	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374489882	chr14:36737766-36737767	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535436549	chr14:36737773-36737774	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554315929	chr14:36737803-36737804	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs188940221	chr14:36737845-36737846	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs568974549	chr14:36737880-36737881	Enhancers Weak transcription Bivalent Enhancer	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:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36720000-36736600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:36735400-36736600	Enhancers	K562	blood
3	chr14:36736200-36736800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:36736400-36737200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr14:36736400-36738000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr14:36736400-36738000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
7	chr14:36736600-36737000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:36736600-36738000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr14:36736600-36738000	Enhancers	Brain Germinal Matrix	brain
10	chr14:36736600-36738800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:36736600-36739600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr14:36736600-36740200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:36736600-36740400	Weak transcription	K562	blood
14	chr14:36736800-36737000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr14:36736800-36737200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:36736800-36738200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr14:36737000-36737200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:36737000-36737600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
19	chr14:36737000-36737800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
20	chr14:36737000-36739400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:36737000-36741000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr14:36737000-36741600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr14:36737200-36738000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:36737200-36738000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:36737200-36738200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr14:36737600-36740600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:36737800-36740600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr14:36738000-36738200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:36738000-36738400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:36738000-36738400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr14:36738000-36738600	Weak transcription	Brain Germinal Matrix	brain
32	chr14:36738000-36738800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr14:36738000-36739000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:36738000-36740800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:36738200-36738600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr14:36738200-36738600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr14:36738200-36739200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:36738200-36740600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr14:36738400-36738600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr14:36738400-36738600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:36738400-36739000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr14:36738600-36738800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:36738600-36738800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr14:36738600-36739000	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr14:36738600-36739200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:36738600-36739400	Enhancers	Brain Germinal Matrix	brain
47	chr14:36738600-36740600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:36738800-36739000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr14:36738800-36739000	Bivalent Enhancer	Fetal Lung	lung
50	chr14:36738800-36739200	Bivalent Enhancer	Fetal Brain Male	brain

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