Variant report

Variant	esv3388652
Chromosome Location	chr15:56534210-56537808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:674)
CpG islands
(count:733)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56536076-56536163	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:56537076-56537557	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:56536596-56536653	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:56536168-56536195	K562	blood:	n/a	n/a
5	ARID3A	chr15:56537020-56537220	K562	blood:	n/a	n/a
6	BACH1	chr15:56536051-56536700	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:56535051-56535346	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr15:56536002-56536363	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:56537304-56537686	K562	blood:	n/a	n/a
10	BHLHE40	chr15:56537299-56538778	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:56536048-56536857	K562	blood:	n/a	chr15:56536222-56536238
12	BHLHE40	chr15:56535713-56536236	HepG2	liver:	n/a	chr15:56535763-56535779 chr15:56535787-56535803
13	BHLHE40	chr15:56536034-56536586	GM12878	blood:	n/a	chr15:56536222-56536238
14	BRCA1	chr15:56536767-56536852	GM12878	blood:	n/a	n/a
15	BRCA1	chr15:56536289-56536304	HepG2	liver:	n/a	n/a
16	CCNT2	chr15:56535344-56536615	K562	blood:	n/a	n/a
17	CEBPB	chr15:56537516-56537768	H1-hESC	embryonic stem cell:	n/a	chr15:56537605-56537616
18	CEBPB	chr15:56537448-56538941	Hela-S3	cervix:	n/a	chr15:56538784-56538797 chr15:56538666-56538679 chr15:56537605-56537616 chr15:56538786-56538795 chr15:56538784-56538795 chr15:56538785-56538796
19	CEBPB	chr15:56537430-56539012	K562	blood:	n/a	chr15:56538784-56538797 chr15:56538666-56538679 chr15:56537605-56537616 chr15:56538786-56538795 chr15:56538784-56538795 chr15:56538785-56538796
20	CEBPB	chr15:56536036-56536187	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:56537432-56537801	HepG2	liver:	n/a	chr15:56537605-56537616
22	CEBPD	chr15:56536772-56536983	HepG2	liver:	n/a	n/a
23	CEBPD	chr15:56535923-56536314	HepG2	liver:	n/a	n/a
24	CEBPD	chr15:56537099-56537650	HepG2	liver:	n/a	n/a
25	CHD1	chr15:56535394-56535402	GM12878	blood:	n/a	n/a
26	CHD1	chr15:56534456-56535045	GM12878	blood:	n/a	n/a
27	CHD1	chr15:56535610-56535867	GM12878	blood:	n/a	n/a
28	CHD1	chr15:56537184-56537361	GM12878	blood:	n/a	n/a
29	CHD1	chr15:56536107-56536617	GM12878	blood:	n/a	n/a
30	CHD1	chr15:56534856-56535219	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr15:56536287-56536600	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr15:56535395-56535454	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr15:56535598-56535813	K562	blood:	n/a	n/a
34	CHD2	chr15:56535313-56536643	GM12878	blood:	n/a	n/a
35	CHD2	chr15:56537405-56537634	K562	blood:	n/a	n/a
36	CHD2	chr15:56536154-56536814	K562	blood:	n/a	n/a
37	CHD2	chr15:56537527-56537646	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr15:56536711-56537144	HepG2	liver:	n/a	n/a
39	CHD2	chr15:56536859-56537672	GM12878	blood:	n/a	n/a
40	CHD2	chr15:56536209-56537338	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr15:56535368-56536438	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr15:56536408-56536793	A549	lung:	n/a	n/a
43	CREB1	chr15:56536018-56536355	A549	lung:	n/a	n/a
44	CREB1	chr15:56535590-56535992	A549	lung:	n/a	n/a
45	CTBP2	chr15:56535288-56537528	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr15:56535600-56535750	HepG2	liver:	n/a	n/a
47	CTCF	chr15:56536040-56536190	AG04449	skin:	n/a	n/a
48	CTCF	chr15:56536913-56536961	Fibrobl	skin:	n/a	n/a
49	CTCF	chr15:56536048-56536271	GM19238	blood:	n/a	n/a
50	CTCF	chr15:56536047-56536250	MCF-7	breast:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56535833-56535883	MCF-7	breast:	n/a
2	chr15:56535833-56535883	MCF-7	breast:	n/a
3	chr15:56536865-56536915	GM06990	blood:	n/a
4	chr15:56535674-56535724	SK-N-SH	brain:	n/a
5	chr15:56535833-56535883	HUVEC	blood vessel:	n/a
6	chr15:56535674-56535724	HRCEpiC	kidney:	n/a
7	chr15:56537579-56537629	NHDF-neo	bronchial:	n/a
8	chr15:56536865-56536915	NH-A	brain:	n/a
9	chr15:56535833-56535883	HIPEpiC	eye:	n/a
10	chr15:56535304-56535354	HEEpiC	esophagus:	n/a
11	chr15:56536865-56536915	PFSK-1	brain:	n/a
12	chr15:56536366-56536416	NHBE	bronchial:	n/a
13	chr15:56535833-56535883	ProgFib	skin:	n/a
14	chr15:56535304-56535354	H1-hESC	embryonic stem cell:	embryo
15	chr15:56536071-56536121	CMK	blood:	n/a
16	chr15:56536865-56536915	MCF-7	breast:	n/a
17	chr15:56536071-56536121	BE2_C	brain:	n/a
18	chr15:56537579-56537629	Hepatocyte	liver:	n/a
19	chr15:56536599-56536649	HUVEC	blood vessel:	n/a
20	chr15:56535833-56535883	HL-60	blood:	n/a
21	chr15:56536599-56536649	HRCEpiC	kidney:	n/a
22	chr15:56536718-56536768	BE2_C	brain:	n/a
23	chr15:56536865-56536915	BJ	skin:	n/a
24	chr15:56535674-56535724	HEEpiC	esophagus:	n/a
25	chr15:56537579-56537629	U87	brain:	n/a
26	chr15:56535484-56535534	HPAEpiC	pulmonary alveolar:	n/a
27	chr15:56535934-56535984	HL-60	blood:	n/a
28	chr15:56535304-56535354	Jurkat	blood:	n/a
29	chr15:56537579-56537629	GM12892	blood:	n/a
30	chr15:56536865-56536915	HRCEpiC	kidney:	n/a
31	chr15:56535304-56535354	IMR90	lung:	fetal
32	chr15:56536071-56536121	T-47D	breast:	n/a
33	chr15:56536718-56536768	CMK	blood:	n/a
34	chr15:56537579-56537629	PANC-1	pancreas:	n/a
35	chr15:56535674-56535724	SKMC	muscle:	n/a
36	chr15:56535833-56535883	HAEpiC	amniotic membrane:	n/a
37	chr15:56537579-56537629	HRE	kidney:	n/a
38	chr15:56536562-56536612	HUVEC	blood vessel:	n/a
39	chr15:56535304-56535354	HNPCEpiC	eye:	n/a
40	chr15:56535484-56535534	AG04450	lung:	fetal
41	chr15:56536599-56536649	HEK293	kidney:	embryo
42	chr15:56536865-56536915	Hela-S3	cervix:	n/a
43	chr15:56535304-56535354	NT2-D1	testis:	n/a
44	chr15:56537579-56537629	K562	blood:	n/a
45	chr15:56537579-56537629	HAEpiC	amniotic membrane:	n/a
46	chr15:56536562-56536612	HRPEpiC	eye:	n/a
47	chr15:56536071-56536121	SK-N-MC	brain:	n/a
48	chr15:56536366-56536416	SKMC	muscle:	n/a
49	chr15:56535833-56535883	K562	blood:	n/a
50	chr15:56536718-56536768	SK-N-SH	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56535646..56536454-chr17:18761002..18761940,2	Hela-S3	cervix:
2	chr15:56535634..56538355-chr15:56656475..56659064,2	MCF-7	breast:
3	chr15:56535585..56536155-chr20:25371606..25372213,2	Hela-S3	cervix:
4	chr15:56483194..56486063-chr15:56535825..56539303,3	MCF-7	breast:
5	chr15:56285427..56286973-chr15:56537527..56538833,7	MCF-7	breast:
6	chr15:56478637..56480315-chr15:56536798..56538580,2	K562	blood:
7	chr15:56282050..56287467-chr15:56534024..56538662,8	MCF-7	breast:
8	chr15:56285499..56287418-chr15:56534884..56536553,2	K562	blood:
9	chr15:56536601..56538445-chr15:57177718..57180315,2	K562	blood:
10	chr15:56536393..56538517-chr15:56614478..56617229,2	MCF-7	breast:
11	chr11:2545295..2546795-chr15:56536741..56538582,2	K562	blood:
12	chr15:56536135..56536920-chr17:43393972..43394515,2	NB4	blood:
13	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
14	chr15:56285813..56288695-chr15:56536371..56538059,2	MCF-7	breast:
15	chr1:147806244..147806949-chr15:56536135..56536885,2	NB4	blood:
16	chr15:56534684..56537162-chr15:57025486..57027553,2	MCF-7	breast:
17	chr15:56536983..56539715-chr15:56539921..56543667,5	K562	blood:
18	chr15:55834428..55836953-chr15:56536453..56538262,2	K562	blood:
19	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:

No data

Variant related genes	Relation type
RFX7	TF binding region
TEX9	TF binding region
RFX7	CpG island
TEX9	CpG island
ENSG00000100997	chromatin interactions
ENSG00000141127	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000261072	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000006062	chromatin interactions
ENSG00000261174	chromatin interactions
ENSG00000151575	chromatin interactions

Extended variants
information (count: 136 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74017496	chr15:56534245-56534246	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576144186	chr15:56534353-56534354	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs545325039	chr15:56534413-56534414	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560456462	chr15:56534432-56534433	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531270056	chr15:56534434-56534435	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370816367	chr15:56534480-56534481	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550588664	chr15:56534503-56534504	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2414471	chr15:56534504-56534505	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs532795462	chr15:56534511-56534512	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546635089	chr15:56534520-56534521	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140003393	chr15:56534541-56534542	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs367955584	chr15:56534546-56534547	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs548798824	chr15:56534573-56534574	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs370427591	chr15:56534582-56534583	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs73411522	chr15:56534589-56534590	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184402553	chr15:56534604-56534605	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs557632615	chr15:56534635-56534636	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs117683028	chr15:56534677-56534678	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs199726084	chr15:56534696-56534697	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs2414472	chr15:56534724-56534725	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs144986498	chr15:56534757-56534758	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs62044144	chr15:56534903-56534904	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs542429819	chr15:56534913-56534914	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs115412779	chr15:56534921-56534922	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs78536030	chr15:56534954-56534955	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs147141408	chr15:56534982-56534983	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs187250026	chr15:56535033-56535034	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs111226902	chr15:56535038-56535039	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546301160	chr15:56535046-56535047	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs191617854	chr15:56535056-56535057	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs529019346	chr15:56535080-56535081	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs548763098	chr15:56535083-56535084	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs2460649	chr15:56535174-56535175	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs531410483	chr15:56535212-56535213	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs551225765	chr15:56535219-56535220	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs140399955	chr15:56535241-56535242	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs61587652	chr15:56535254-56535255	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs61262976	chr15:56535261-56535262	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs553123862	chr15:56535264-56535265	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs566948954	chr15:56535306-56535307	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369458958	chr15:56535316-56535317	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373222803	chr15:56535341-56535342	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs376360525	chr15:56535352-56535353	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369905644	chr15:56535382-56535383	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs536003334	chr15:56535426-56535427	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs372966380	chr15:56535447-56535448	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs1996676	chr15:56535491-56535492	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs555902124	chr15:56535763-56535764	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs575868488	chr15:56535781-56535782	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs566907757	chr15:56535839-56535840	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56508000-56534400	Weak transcription	Fetal Heart	heart
2	chr15:56514000-56535000	Weak transcription	Pancreas	Pancrea
3	chr15:56514800-56534800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr15:56524600-56534800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:56524800-56534800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:56524800-56534800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr15:56524800-56534800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr15:56524800-56534800	Weak transcription	Small Intestine	intestine
9	chr15:56524800-56535000	Weak transcription	Esophagus	oesophagus
10	chr15:56525400-56534800	Weak transcription	Placenta	Placenta
11	chr15:56525400-56535000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:56525600-56535000	Weak transcription	Lung	lung
13	chr15:56529400-56535000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:56530600-56534600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr15:56531400-56535000	Weak transcription	Left Ventricle	heart
16	chr15:56532000-56537000	Active TSS	GM12878-XiMat	blood
17	chr15:56532400-56537000	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr15:56532600-56534400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:56532600-56537000	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr15:56532600-56537000	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr15:56532600-56537000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr15:56532600-56537000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr15:56532600-56537000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:56532600-56537000	Active TSS	HMEC	breast
25	chr15:56533000-56537000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:56533200-56534600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr15:56533200-56534800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr15:56533200-56535200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr15:56533200-56536800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:56533200-56537000	Active TSS	H1 Cell Line	embryonic stem cell
31	chr15:56533200-56537000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr15:56533200-56537200	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr15:56533400-56534400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr15:56533400-56534600	Flanking Active TSS	Primary T cells from cord blood	blood
35	chr15:56533400-56534600	Flanking Active TSS	HUVEC	blood vessel
36	chr15:56533400-56534800	Enhancers	Liver	Liver
37	chr15:56533400-56534800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr15:56533400-56534800	Enhancers	Fetal Intestine Small	intestine
39	chr15:56533400-56535200	Active TSS	Fetal Brain Male	brain
40	chr15:56533400-56536200	Active TSS	HSMMtube	muscle
41	chr15:56533400-56536400	Active TSS	NHEK	skin
42	chr15:56533400-56536600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:56533400-56536800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr15:56533400-56536800	Active TSS	K562	blood
45	chr15:56533400-56536800	Active TSS	NHDF-Ad	bronchial
46	chr15:56533400-56537000	Active TSS	Thymus	Thymus
47	chr15:56533400-56537000	Active TSS	NHLF	lung
48	chr15:56533400-56537200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:56533400-56537200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr15:56533400-56537200	Active TSS	Brain Germinal Matrix	brain

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