Variant report

Variant	esv1807328
Chromosome Location	chr15:42525300-42573278
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:832)
CpG islands
(count:1528)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42566680-42567011	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:42565103-42566342	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:42567248-42567519	K562	blood:	n/a	n/a
4	ATF1	chr15:42565151-42566153	K562	blood:	n/a	n/a
5	ATF2	chr15:42565128-42565962	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:42565240-42566091	GM12878	blood:	n/a	n/a
7	ATF2	chr15:42565220-42565693	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:42565086-42565735	GM12878	blood:	n/a	n/a
9	BACH1	chr15:42566258-42566267	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:42571559-42571922	K562	blood:	n/a	n/a
11	BACH1	chr15:42565191-42565854	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr15:42565205-42565682	A549	lung:	n/a	n/a
13	BCL3	chr15:42565289-42565851	A549	lung:	n/a	n/a
14	BCLAF1	chr15:42565086-42566518	GM12878	blood:	n/a	n/a
15	BCLAF1	chr15:42565125-42566650	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:42565232-42566680	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:42571337-42572085	K562	blood:	n/a	n/a
18	BHLHE40	chr15:42565191-42567220	K562	blood:	n/a	n/a
19	BHLHE40	chr15:42565375-42566126	HepG2	liver:	n/a	n/a
20	BRCA1	chr15:42565405-42565896	HepG2	liver:	n/a	n/a
21	BRCA1	chr15:42564908-42565775	H1-hESC	embryonic stem cell:	n/a	chr15:42565231-42565238
22	BRCA1	chr15:42566532-42566636	HepG2	liver:	n/a	n/a
23	BRCA1	chr15:42566234-42566325	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr15:42564758-42566829	Hela-S3	cervix:	n/a	chr15:42565231-42565238
25	CBX3	chr15:42565071-42566044	K562	blood:	n/a	n/a
26	CBX3	chr15:42571335-42572016	K562	blood:	n/a	n/a
27	CBX3	chr15:42544053-42544417	K562	blood:	n/a	n/a
28	CCNT2	chr15:42565279-42566034	K562	blood:	n/a	chr15:42565403-42565412 chr15:42565344-42565353 chr15:42565934-42565943
29	CCNT2	chr15:42566384-42566666	K562	blood:	n/a	n/a
30	CEBPB	chr15:42571320-42571809	K562	blood:	n/a	n/a
31	CEBPB	chr15:42566155-42566349	K562	blood:	n/a	n/a
32	CEBPB	chr15:42571324-42571824	K562	blood:	n/a	n/a
33	CEBPB	chr15:42565228-42565594	HepG2	liver:	n/a	n/a
34	CEBPB	chr15:42565237-42565617	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr15:42565306-42565601	K562	blood:	n/a	n/a
36	CEBPB	chr15:42559546-42559752	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:42568215-42568518	K562	blood:	n/a	n/a
38	CEBPB	chr15:42565218-42565803	K562	blood:	n/a	n/a
39	CEBPB	chr15:42571365-42571672	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:42568214-42568580	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:42568246-42568548	HepG2	liver:	n/a	n/a
42	CEBPB	chr15:42565107-42566642	Hela-S3	cervix:	n/a	chr15:42566454-42566465
43	CEBPB	chr15:42571415-42571609	K562	blood:	n/a	n/a
44	CEBPB	chr15:42571448-42571608	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:42559547-42559842	IMR90	lung:	n/a	n/a
46	CEBPD	chr15:42565099-42565889	K562	blood:	n/a	n/a
47	CEBPD	chr15:42565306-42566051	HepG2	liver:	n/a	n/a
48	CHD1	chr15:42566626-42566754	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr15:42564623-42565634	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr15:42565859-42566167	H1-hESC	embryonic stem cell:	n/a	chr15:42565927-42565937

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42565284-42565334	PFSK-1	brain:	n/a
2	chr15:42565830-42565880	U87	brain:	n/a
3	chr15:42566151-42566201	GM12878	blood:	n/a
4	chr15:42565284-42565334	PFSK-1	brain:	n/a
5	chr15:42565830-42565880	U87	brain:	n/a
6	chr15:42566151-42566201	GM12878	blood:	n/a
7	chr15:42566151-42566201	BJ	skin:	n/a
8	chr15:42565784-42565834	IMR90	lung:	fetal
9	chr15:42565790-42565840	U87	brain:	n/a
10	chr15:42565651-42565701	GM12878	blood:	n/a
11	chr15:42550398-42550448	GM06990	blood:	n/a
12	chr15:42566318-42566368	BE2_C	brain:	n/a
13	chr15:42565830-42565880	T-47D	breast:	n/a
14	chr15:42566264-42566314	ovcar-3	ovarian:	n/a
15	chr15:42565522-42565572	AG04449	skin:	fetal
16	chr15:42566300-42566350	AG04449	skin:	fetal
17	chr15:42565784-42565834	GM19239	blood:	n/a
18	chr15:42565872-42565922	HepG2	liver:	n/a
19	chr15:42566272-42566322	NT2-D1	testis:	n/a
20	chr15:42566264-42566314	BE2_C	brain:	n/a
21	chr15:42568411-42568461	AG09319	gingival:	n/a
22	chr15:42566390-42566440	IMR90	lung:	fetal
23	chr15:42566203-42566253	SAEC	small airway:	n/a
24	chr15:42565790-42565840	IMR90	lung:	fetal
25	chr15:42562638-42562688	U87	brain:	n/a
26	chr15:42566662-42566712	H1-hESC	embryonic stem cell:	embryo
27	chr15:42565830-42565880	ECC-1	luminal epithelium:	n/a
28	chr15:42566318-42566368	LNCaP	prostate:	n/a
29	chr15:42566662-42566712	GM12891	blood:	n/a
30	chr15:42565651-42565701	BE2_C	brain:	n/a
31	chr15:42565760-42565810	SAEC	small airway:	n/a
32	chr15:42565522-42565572	NT2-D1	testis:	n/a
33	chr15:42566318-42566368	A549	lung:	n/a
34	chr15:42566343-42566393	A549	lung:	n/a
35	chr15:42566151-42566201	AG10803	skin:	n/a
36	chr15:42566151-42566201	HL-60	blood:	n/a
37	chr15:42566151-42566201	NT2-D1	testis:	n/a
38	chr15:42565903-42565953	U87	brain:	n/a
39	chr15:42568411-42568461	HCF	heart:	n/a
40	chr15:42565830-42565880	NT2-D1	testis:	n/a
41	chr15:42565790-42565840	HRE	kidney:	n/a
42	chr15:42566151-42566201	HIPEpiC	eye:	n/a
43	chr15:42566390-42566440	MCF10A-Er-Src	breast:	n/a
44	chr15:42565790-42565840	Hepatocyte	liver:	n/a
45	chr15:42566272-42566322	CMK	blood:	n/a
46	chr15:42566390-42566440	GM12878	blood:	n/a
47	chr15:42566343-42566393	HCF	heart:	n/a
48	chr15:42568411-42568461	SKMC	muscle:	n/a
49	chr15:42565522-42565572	NB4	blood:	n/a
50	chr15:42566203-42566253	NT2-D1	testis:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42565177..42566160-chr3:69062410..69063138,2	Hela-S3	cervix:
2	chr15:42519855..42522607-chr15:42524004..42525780,2	K562	blood:
3	chr15:42565208..42566147-chr19:48824795..48825577,2	NB4	blood:
4	chr15:42553565..42555968-chr15:42563813..42566257,3	MCF-7	breast:
5	chr15:42563158..42565885-chr15:42567865..42572400,4	MCF-7	breast:
6	chr14:77923503..77924384-chr15:42565241..42565896,2	NB4	blood:
7	chr10:58120889..58121499-chr15:42565318..42565842,2	Hela-S3	cervix:
8	chr15:42565452..42566007-chr6:13328640..13329262,2	Hela-S3	cervix:
9	chr15:42544015..42546634-chr15:42547457..42549970,2	K562	blood:
10	chr15:42564714..42568797-chr15:42571510..42577176,8	K562	blood:
11	chr11:34073237..34073837-chr15:42565350..42566240,2	Hela-S3	cervix:
12	chr11:62554539..62555349-chr15:42565272..42566248,2	Hela-S3	cervix:
13	chr15:42563255..42565132-chr15:42636659..42638368,2	K562	blood:
14	chr15:42498938..42502268-chr15:42564432..42567193,3	MCF-7	breast:
15	chr1:115212876..115213635-chr15:42565277..42565911,2	Hela-S3	cervix:
16	chr15:42533593..42536142-chr15:42545624..42547945,2	K562	blood:
17	chr15:42565092..42565818-chr7:107384648..107385356,2	Hela-S3	cervix:
18	chr15:42565305..42567163-chr15:42839364..42842481,3	K562	blood:
19	chr15:42533593..42536142-chr15:42545624..42547945,2	K562	blood:
20	chr15:42565172..42565968-chr3:20227231..20227766,2	Hela-S3	cervix:
21	chr15:42532284..42534911-chr15:42549043..42552041,2	K562	blood:
22	chr15:42568979..42570543-chr15:42572513..42574015,2	K562	blood:
23	chr15:42563158..42565885-chr15:42567865..42572400,4	MCF-7	breast:
24	chr15:42550561..42553177-chr15:42566692..42569235,2	K562	blood:
25	chr15:42564172..42566903-chr15:42569265..42571976,2	MCF-7	breast:
26	chr15:42559733..42563310-chr15:42678634..42681534,3	K562	blood:
27	chr15:42544015..42546634-chr15:42547457..42549970,2	K562	blood:
28	chr1:147806312..147807083-chr15:42565139..42566022,2	Hela-S3	cervix:
29	chr11:71814032..71814862-chr15:42565436..42566128,2	NB4	blood:
30	chr15:42515383..42517801-chr15:42527177..42529552,2	K562	blood:
31	chr15:42568840..42573155-chr15:42578082..42582332,4	K562	blood:
32	chr15:42554958..42556524-chr15:42720183..42722144,2	K562	blood:
33	chr15:42545753..42549905-chr15:42563424..42566580,4	K562	blood:
34	chr15:42565191..42565693-chr4:25378475..25379333,2	Hela-S3	cervix:
35	chr15:42499099..42501734-chr15:42564008..42565710,2	K562	blood:
36	chr15:42547199..42549905-chr15:42563424..42565633,2	K562	blood:
37	chr15:42552126..42554806-chr15:42568266..42570874,3	MCF-7	breast:
38	chr15:42565726..42566604-chr15:65588308..65589204,2	Hela-S3	cervix:
39	chr13:96328903..96329487-chr15:42565285..42566134,2	Hela-S3	cervix:
40	chr1:155903773..155904358-chr15:42565120..42565881,2	Hela-S3	cervix:
41	chr15:42532284..42534911-chr15:42549043..42552041,2	K562	blood:
42	chr15:42565173..42566146-chr19:17829994..17830507,2	HCT-116	colon:
43	chr15:42564636..42566534-chr15:42781561..42783413,2	K562	blood:
44	chr15:42568979..42570543-chr15:42572513..42574015,2	K562	blood:
45	chr15:42453296..42455922-chr15:42565346..42568176,2	K562	blood:
46	chr15:42544904..42547005-chr15:42561537..42563318,2	K562	blood:
47	chr15:42544904..42547005-chr15:42561537..42563318,2	K562	blood:
48	chr15:42523615..42525388-chr15:42565299..42567671,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM87A	hsa-miR-30a-5p	chr15:42525358-42525378

Variant related genes	Relation type
GANC	TF binding region
TMEM87A	TF binding region
GANC	CpG island
TMEM87A	CpG island
ENSG00000199568	chromatin interactions
ENSG00000103994	chromatin interactions
ENSG00000247400	chromatin interactions
ENSG00000166887	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000102580	chromatin interactions
ENSG00000180979	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000163378	chromatin interactions
ENSG00000103978	chromatin interactions
ENSG00000214013	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000105879	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000244513	chromatin interactions
ENSG00000100591	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000175984	chromatin interactions
ENSG00000053900	chromatin interactions
ENSG00000130479	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000151445	chromatin interactions
ENSG00000185475	chromatin interactions
ENSG00000241764	chromatin interactions
ENSG00000137814	chromatin interactions
ENSG00000135387	chromatin interactions
ENSG00000261002	chromatin interactions
ENSG00000122952	chromatin interactions

Extended variants
information (count: 1929 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56833829	chr15:42525313-42525314	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs568302254	chr15:42525317-42525318	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs79255138	chr15:42525329-42525330	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200929706	chr15:42525367-42525368	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
5	rs368413075	chr15:42525384-42525385	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371881218	chr15:42525477-42525478	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368001919	chr15:42525535-42525536	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570469838	chr15:42525551-42525552	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140721007	chr15:42525590-42525591	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs77188091	chr15:42525618-42525619	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575988953	chr15:42525683-42525684	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113711505	chr15:42525686-42525687	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566352402	chr15:42525803-42525804	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs4924636	chr15:42525809-42525810	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs555627149	chr15:42525841-42525842	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs572335309	chr15:42525855-42525856	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs541246174	chr15:42525870-42525871	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs111979580	chr15:42525872-42525873	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs536977300	chr15:42525890-42525891	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187355167	chr15:42525898-42525899	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368806023	chr15:42525919-42525920	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548887709	chr15:42525951-42525952	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35571344	chr15:42525965-42525966	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145910130	chr15:42525984-42525985	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569507304	chr15:42525985-42525986	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372969720	chr15:42526000-42526001	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112609122	chr15:42526020-42526021	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529294404	chr15:42526043-42526044	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548536415	chr15:42526060-42526061	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs8041101	chr15:42526092-42526093	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs199915065	chr15:42526101-42526102	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114769781	chr15:42526127-42526128	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11285848	chr15:42526136-42526137	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76806048	chr15:42526152-42526153	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558361688	chr15:42526194-42526195	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184772607	chr15:42526224-42526225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570579953	chr15:42526271-42526272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539207749	chr15:42526282-42526283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375937208	chr15:42526309-42526310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187660934	chr15:42526328-42526329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569587057	chr15:42526356-42526357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535063327	chr15:42526364-42526365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111282363	chr15:42526388-42526389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554913097	chr15:42526433-42526434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74009028	chr15:42526461-42526462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541283918	chr15:42526485-42526486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376949901	chr15:42526499-42526500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558069120	chr15:42526591-42526592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs36083087	chr15:42526638-42526639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148551021	chr15:42526686-42526687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Intracranial arachnoid cysts	20187927	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1963 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42500800-42563200	Weak transcription	Stomach Mucosa	stomach
2	chr15:42501000-42534800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:42501000-42536600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:42501000-42536800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr15:42501000-42538000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr15:42501200-42532400	Strong transcription	Fetal Muscle Trunk	muscle
7	chr15:42501800-42536800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr15:42502000-42535000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:42502200-42534000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:42502200-42536600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr15:42502800-42535200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:42502800-42536400	Strong transcription	Fetal Muscle Leg	muscle
13	chr15:42503200-42544000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:42506800-42532000	Strong transcription	Placenta	Placenta
15	chr15:42508000-42532200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr15:42509400-42535200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:42511800-42536800	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr15:42513200-42532200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr15:42513800-42534800	Strong transcription	Liver	Liver
20	chr15:42514000-42526600	Strong transcription	Left Ventricle	heart
21	chr15:42514000-42534800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr15:42514000-42535200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr15:42514200-42526600	Strong transcription	Duodenum Smooth Muscle	Duodenum
24	chr15:42514200-42527000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr15:42514200-42532400	Strong transcription	Adipose Nuclei	Adipose
26	chr15:42514200-42535200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:42514200-42535200	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr15:42514400-42531800	Strong transcription	Primary T cells from cord blood	blood
29	chr15:42514400-42533600	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr15:42514400-42534800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr15:42514400-42535000	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr15:42514400-42535000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:42514400-42536400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr15:42514400-42536400	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr15:42514400-42537200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr15:42514600-42535000	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr15:42514800-42532000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr15:42515000-42535400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr15:42515000-42544600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr15:42515200-42526400	Strong transcription	Primary hematopoietic stem cells	blood
41	chr15:42515200-42526800	Strong transcription	Brain Anterior Caudate	brain
42	chr15:42515200-42534800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr15:42515400-42535400	Strong transcription	Primary T helper cells PMA-I stimulated	--
44	chr15:42515600-42525600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:42515600-42526800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr15:42515600-42530400	Strong transcription	NH-A	brain
47	chr15:42515600-42532600	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr15:42515600-42535000	Strong transcription	Primary B cells from cord blood	blood
49	chr15:42515800-42532400	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr15:42516000-42535200	Strong transcription	Primary B cells from peripheral blood	blood

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