Variant report

Variant	nsv904218
Chromosome Location	chr15:51743186-51873407
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	chr15:51872535-51873050	K562	blood:	n/a	n/a
2	ARID3A	chr15:51777123-51777159	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:51829219-51829543	K562	blood:	n/a	n/a
4	ARID3A	chr15:51871485-51871486	K562	blood:	n/a	n/a
5	ARID3A	chr15:51870029-51870641	K562	blood:	n/a	n/a
6	ARID3A	chr15:51869305-51869743	K562	blood:	n/a	n/a
7	ARID3A	chr15:51785803-51787439	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:51762752-51763140	HepG2	liver:	n/a	n/a
9	ATF1	chr15:51872652-51872968	K562	blood:	n/a	n/a
10	ATF1	chr15:51869224-51869631	K562	blood:	n/a	n/a
11	BACH1	chr15:51837448-51837464	K562	blood:	n/a	n/a
12	BATF	chr15:51826141-51826489	GM12878	blood:	n/a	chr15:51826320-51826331
13	BHLHE40	chr15:51868654-51868977	K562	blood:	n/a	n/a
14	BHLHE40	chr15:51861393-51861769	K562	blood:	n/a	n/a
15	BRCA1	chr15:51827521-51827564	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr15:51859110-51859141	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr15:51777015-51777300	K562	blood:	n/a	n/a
18	CBX3	chr15:51776958-51777361	K562	blood:	n/a	n/a
19	CCNT2	chr15:51870168-51870404	K562	blood:	n/a	n/a
20	CCNT2	chr15:51834574-51834704	K562	blood:	n/a	n/a
21	CCNT2	chr15:51872739-51873018	K562	blood:	n/a	n/a
22	CEBPB	chr15:51868691-51869675	MCF-7	breast:	n/a	chr15:51869180-51869191
23	CEBPB	chr15:51868703-51869797	MCF-7	breast:	n/a	chr15:51869180-51869191
24	CEBPB	chr15:51786177-51786317	HepG2	liver:	n/a	n/a
25	CEBPB	chr15:51871259-51871628	Hela-S3	cervix:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
26	CEBPB	chr15:51868987-51869626	Hela-S3	cervix:	n/a	chr15:51869180-51869191
27	CEBPB	chr15:51868972-51869542	K562	blood:	n/a	chr15:51869180-51869191
28	CEBPB	chr15:51847287-51847351	A549	lung:	n/a	n/a
29	CEBPB	chr15:51858682-51858816	A549	lung:	n/a	chr15:51858795-51858812 chr15:51858798-51858811
30	CEBPB	chr15:51871143-51871792	A549	lung:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
31	CEBPB	chr15:51868997-51869387	A549	lung:	n/a	chr15:51869180-51869191
32	CEBPB	chr15:51871156-51871628	MCF-7	breast:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
33	CEBPB	chr15:51869020-51869387	IMR90	lung:	n/a	chr15:51869180-51869191
34	CEBPB	chr15:51847213-51847445	MCF-7	breast:	n/a	n/a
35	CEBPB	chr15:51868917-51869369	A549	lung:	n/a	chr15:51869180-51869191
36	CEBPB	chr15:51871207-51871597	ECC-1	luminal epithelium:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
37	CEBPB	chr15:51780941-51781263	IMR90	lung:	n/a	chr15:51781121-51781132
38	CEBPB	chr15:51761814-51762007	IMR90	lung:	n/a	chr15:51761907-51761920
39	CEBPB	chr15:51791495-51791801	A549	lung:	n/a	chr15:51791616-51791627
40	CEBPB	chr15:51772156-51772419	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:51871245-51871623	HepG2	liver:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
42	CEBPB	chr15:51871245-51871622	IMR90	lung:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
43	CEBPB	chr15:51871260-51871554	ECC-1	luminal epithelium:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
44	CEBPB	chr15:51871247-51871617	A549	lung:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
45	CEBPB	chr15:51787035-51787419	MCF-7	breast:	n/a	chr15:51787186-51787197
46	CEBPB	chr15:51869018-51869378	HepG2	liver:	n/a	chr15:51869180-51869191
47	CEBPB	chr15:51871078-51871823	MCF-7	breast:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
48	CEBPB	chr15:51868995-51869361	ECC-1	luminal epithelium:	n/a	chr15:51869180-51869191
49	CEBPB	chr15:51871270-51871610	H1-hESC	embryonic stem cell:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444
50	CEBPB	chr15:51871182-51871639	K562	blood:	n/a	chr15:51871428-51871441 chr15:51871430-51871439 chr15:51871429-51871440 chr15:51871430-51871439 chr15:51871430-51871439 chr15:51871427-51871444

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51762495-51762545	H1-hESC	embryonic stem cell:	embryo
2	chr15:51786154-51786204	SK-N-MC	brain:	n/a
3	chr15:51786154-51786204	AG09309	skin:	n/a
4	chr15:51762495-51762545	NT2-D1	testis:	n/a
5	chr15:51786154-51786204	ProgFib	skin:	n/a
6	chr15:51786154-51786204	HCF	heart:	n/a
7	chr15:51786154-51786204	HRPEpiC	eye:	n/a
8	chr15:51762495-51762545	Hepatocyte	liver:	n/a
9	chr15:51762495-51762545	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:51762495-51762545	MCF10A-Er-Src	breast:	n/a
11	chr15:51786154-51786204	Caco-2	colon:	n/a
12	chr15:51786154-51786204	HEEpiC	esophagus:	n/a
13	chr15:51786154-51786204	A549	lung:	n/a
14	chr15:51762495-51762545	ovcar-3	ovarian:	n/a
15	chr15:51786154-51786204	SK-N-SH	brain:	n/a
16	chr15:51762495-51762545	PFSK-1	brain:	n/a
17	chr15:51786154-51786204	RPTEC	kidney:	n/a
18	chr15:51762495-51762545	ProgFib	skin:	n/a
19	chr15:51762495-51762545	SAEC	small airway:	n/a
20	chr15:51762495-51762545	SKMC	muscle:	n/a
21	chr15:51786154-51786204	IMR90	lung:	fetal
22	chr15:51786154-51786204	H1-hESC	embryonic stem cell:	embryo
23	chr15:51786154-51786204	NH-A	brain:	n/a
24	chr15:51762495-51762545	LNCaP	prostate:	n/a
25	chr15:51762495-51762545	SK-N-SH_RA	brain:	n/a
26	chr15:51786154-51786204	SKMC	muscle:	n/a
27	chr15:51786154-51786204	HRE	kidney:	n/a
28	chr15:51786154-51786204	NB4	blood:	n/a
29	chr15:51762495-51762545	HepG2	liver:	n/a
30	chr15:51762495-51762545	HRPEpiC	eye:	n/a
31	chr15:51786154-51786204	GM12892	blood:	n/a
32	chr15:51786154-51786204	HUVEC	blood vessel:	n/a
33	chr15:51762495-51762545	HMEC	breast:	n/a
34	chr15:51762495-51762545	NH-A	brain:	n/a
35	chr15:51762495-51762545	Caco-2	colon:	n/a
36	chr15:51786154-51786204	MCF10A-Er-Src	breast:	n/a
37	chr15:51786154-51786204	AoSMC	blood vessel:	n/a
38	chr15:51786154-51786204	BE2_C	brain:	n/a
39	chr15:51786154-51786204	GM12878	blood:	n/a
40	chr15:51762495-51762545	CMK	blood:	n/a
41	chr15:51762495-51762545	HEEpiC	esophagus:	n/a
42	chr15:51762495-51762545	BE2_C	brain:	n/a
43	chr15:51786154-51786204	PrEC	prostate:	n/a
44	chr15:51762495-51762545	AG10803	skin:	n/a
45	chr15:51786154-51786204	HL-60	blood:	n/a
46	chr15:51762495-51762545	GM12891	blood:	n/a
47	chr15:51762495-51762545	MCF-7	breast:	n/a
48	chr15:51762495-51762545	Jurkat	blood:	n/a
49	chr15:51786154-51786204	HMEC	breast:	n/a
50	chr15:51786154-51786204	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:51872226..51872785-chr8:61590656..61591256,2	NB4	blood:
2	chr15:51813148..51814978-chr15:51814982..51816797,2	MCF-7	breast:
3	chr15:51752661..51754264-chr15:51765649..51768116,2	MCF-7	breast:
4	chr15:51869314..51872893-chr15:51913496..51916376,3	MCF-7	breast:
5	chr15:51843037..51845513-chr15:51854667..51856394,2	K562	blood:
6	chr15:51867811..51869730-chr15:51913400..51915633,2	MCF-7	breast:
7	chr15:51833724..51835640-chr15:51837981..51840584,2	MCF-7	breast:
8	chr15:51828912..51831495-chr15:51835540..51837204,2	K562	blood:
9	chr15:51785271..51787654-chr15:51788490..51790028,2	MCF-7	breast:
10	chr15:51825801..51827615-chr15:51831026..51833180,2	MCF-7	breast:
11	chr15:51695107..51695963-chr15:51791260..51792237,6	MCF-7	breast:
12	chr15:51854337..51857092-chr15:51860809..51862898,2	K562	blood:
13	chr15:51835902..51838646-chr15:51851787..51853381,2	MCF-7	breast:
14	chr15:51813148..51814978-chr15:51814982..51816797,2	MCF-7	breast:
15	chr15:51770845..51772566-chr15:51776340..51779147,2	MCF-7	breast:
16	chr15:51770845..51772566-chr15:51776340..51779147,2	MCF-7	breast:
17	chr15:51833724..51835640-chr15:51837981..51840584,2	MCF-7	breast:
18	chr15:51773834..51778249-chr15:51779820..51782019,4	K562	blood:
19	chr15:51799531..51802188-chr15:51804343..51807032,2	MCF-7	breast:
20	chr15:51861248..51863140-chr15:51914368..51916557,2	MCF-7	breast:
21	chr15:51672962..51673958-chr15:51793026..51793755,2	MCF-7	breast:
22	chr15:51814441..51816242-chr15:51826591..51828165,2	K562	blood:
23	chr15:51855034..51858623-chr15:51869913..51872025,3	MCF-7	breast:
24	chr15:51859933..51862256-chr15:51866857..51869173,2	MCF-7	breast:
25	chr15:51812082..51813725-chr15:51814759..51816922,2	K562	blood:
26	chr15:51797075..51799588-chr15:51799701..51803630,3	MCF-7	breast:
27	chr15:51820517..51823414-chr15:51826309..51828768,2	K562	blood:
28	chr15:51828716..51829794-chr15:51913651..51914977,4	MCF-7	breast:
29	chr15:51837957..51840448-chr15:51845565..51847843,2	K562	blood:
30	chr15:51703226..51705679-chr15:51790257..51792608,2	MCF-7	breast:
31	chr15:51828880..51829850-chr15:51865800..51866794,7	MCF-7	breast:
32	chr15:51811820..51813390-chr15:51823988..51825927,2	K562	blood:
33	chr15:51793814..51797764-chr15:51797866..51800852,4	MCF-7	breast:
34	chr15:51870572..51873309-chr15:51873394..51875007,2	MCF-7	breast:
35	chr15:51796127..51797657-chr15:51807197..51809893,2	MCF-7	breast:
36	chr15:51829420..51832370-chr15:51850921..51852494,2	K562	blood:
37	chr15:51827369..51828145-chr17:43095767..43096349,2	MCF-7	breast:
38	chr15:51830715..51832305-chr15:51842133..51844181,2	K562	blood:
39	chr15:51869903..51873924-chr15:51913633..51916581,3	MCF-7	breast:
40	chr15:51812082..51813725-chr15:51814759..51816922,2	K562	blood:
41	chr15:51857366..51859999-chr15:51867554..51870226,2	MCF-7	breast:
42	chr15:51764721..51766782-chr15:51782028..51783869,2	MCF-7	breast:
43	chr15:51745144..51748040-chr15:51748185..51750918,2	K562	blood:
44	chr15:51833348..51836933-chr15:51844447..51846431,3	MCF-7	breast:
45	chr15:51844973..51847549-chr15:53093703..53095676,2	MCF-7	breast:
46	chr15:51838753..51841141-chr15:51845235..51847701,2	MCF-7	breast:
47	chr15:51828883..51829809-chr15:51853123..51854092,2	MCF-7	breast:
48	chr15:51854337..51857092-chr15:51860809..51862898,2	K562	blood:
49	chr15:51828988..51832305-chr15:51839364..51844181,4	K562	blood:
50	chr15:51791214..51792773-chr15:51798432..51801383,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLDN-2	chr15:51750917-51751126	ENSG00000259668.1
2	lnc-GLDN-2	chr15:51750917-51751126	ENSG00000259668.1
3	lnc-GLDN-3	chr15:51746272-51746336	ENSG00000259678.1
4	lnc-GLDN-3	chr15:51758387-51758520	ENSG00000259678.1
5	lnc-GLDN-2	chr15:51752552-51752763	ENSG00000259668.1
6	lnc-GLDN-3	chr15:51758693-51758726	ENSG00000259678.1
7	lnc-GLDN-2	chr15:51750101-51750250	ENSG00000259668.1
8	lnc-GLDN-2	chr15:51752495-51752764	ENSG00000259668.1
9	lnc-GLDN-3	chr15:51790965-51791030	ENSG00000259678.1
10	lnc-GLDN-2	chr15:51750113-51750250	ENSG00000259668.1

Variant related genes	Relation type
ENSG00000259668	TF binding region
DMXL2	TF binding region
ENSG00000259668	CpG island
DMXL2	CpG island
ENSG00000128872	chromatin interactions
ENSG00000104093	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000259668	chromatin interactions

Extended variants
information (count: 4724 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4724 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17524694	chr15:51743186-51743187	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs193025464	chr15:51743193-51743194	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs538007751	chr15:51743211-51743212	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185556636	chr15:51743220-51743221	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs16964354	chr15:51743255-51743256	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538966486	chr15:51743331-51743332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569929196	chr15:51743347-51743348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78474015	chr15:51743403-51743404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572100277	chr15:51743413-51743414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544071792	chr15:51743456-51743457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554720787	chr15:51743469-51743470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576493327	chr15:51743528-51743529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543218844	chr15:51743584-51743585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541350471	chr15:51743599-51743600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115045631	chr15:51743634-51743635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532377179	chr15:51743683-51743684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139908622	chr15:51743699-51743700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541992828	chr15:51743700-51743701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs16964357	chr15:51743718-51743719	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs529654394	chr15:51743770-51743771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548171560	chr15:51743790-51743791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376130707	chr15:51743798-51743799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370463400	chr15:51743806-51743807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530021803	chr15:51743809-51743810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533524255	chr15:51743811-51743812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569607452	chr15:51743819-51743820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548311682	chr15:51743827-51743828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530642955	chr15:51743833-51743834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549931660	chr15:51743834-51743835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373899284	chr15:51743844-51743845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200751363	chr15:51743848-51743849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377563440	chr15:51743861-51743862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190511003	chr15:51743909-51743910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74013219	chr15:51743936-51743937	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs200955838	chr15:51743941-51743942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184602533	chr15:51743947-51743948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35402836	chr15:51743953-51743954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536215218	chr15:51743972-51743973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370853607	chr15:51743976-51743977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554964436	chr15:51744018-51744019	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143677049	chr15:51744050-51744051	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543878981	chr15:51744095-51744096	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559130381	chr15:51744163-51744164	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577101866	chr15:51744173-51744174	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541273912	chr15:51744215-51744216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559639753	chr15:51744226-51744227	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530011083	chr15:51744274-51744275	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188282573	chr15:51744280-51744281	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181413967	chr15:51744305-51744306	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569832273	chr15:51744327-51744328	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1493 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51734600-51748800	Weak transcription	Fetal Intestine Small	intestine
2	chr15:51736800-51751200	Weak transcription	HUVEC	blood vessel
3	chr15:51737000-51775600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr15:51737000-51776400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr15:51737400-51749000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:51737400-51750200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:51737600-51749200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr15:51737600-51762400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:51737800-51748800	Weak transcription	NHDF-Ad	bronchial
10	chr15:51737800-51758400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:51737800-51762400	Weak transcription	Colonic Mucosa	Colon
12	chr15:51738000-51755400	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr15:51738200-51748800	Weak transcription	Fetal Brain Male	brain
14	chr15:51738200-51784600	Weak transcription	Stomach Mucosa	stomach
15	chr15:51738400-51777400	Weak transcription	Small Intestine	intestine
16	chr15:51738600-51743400	Strong transcription	Brain Inferior Temporal Lobe	brain
17	chr15:51738600-51744600	Strong transcription	Adipose Nuclei	Adipose
18	chr15:51738600-51751800	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr15:51738800-51743400	Strong transcription	Placenta	Placenta
20	chr15:51738800-51744600	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr15:51738800-51752000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr15:51738800-51752200	Strong transcription	Fetal Intestine Large	intestine
23	chr15:51738800-51752600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr15:51739000-51749400	Weak transcription	GM12878-XiMat	blood
25	chr15:51739000-51750200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:51739000-51752000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr15:51739000-51752000	Strong transcription	Liver	Liver
28	chr15:51739000-51776000	Weak transcription	Gastric	stomach
29	chr15:51739200-51744400	Strong transcription	Duodenum Smooth Muscle	Duodenum
30	chr15:51739200-51746800	Weak transcription	Right Ventricle	heart
31	chr15:51739200-51748800	Weak transcription	Osteobl	bone
32	chr15:51739400-51743400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr15:51739400-51744800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr15:51739400-51747200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr15:51739400-51747600	Weak transcription	Ovary	ovary
36	chr15:51739600-51743600	Strong transcription	HSMM	muscle
37	chr15:51739800-51744000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr15:51740200-51743400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:51740200-51751800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr15:51740600-51751800	Weak transcription	Psoas Muscle	Psoas
41	chr15:51740800-51775200	Weak transcription	Pancreas	Pancrea
42	chr15:51741000-51743200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr15:51741000-51743400	Strong transcription	Dnd41	blood
44	chr15:51741000-51753200	Weak transcription	HepG2	liver
45	chr15:51741200-51743600	Strong transcription	Fetal Brain Female	brain
46	chr15:51741200-51751000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr15:51741400-51746800	Weak transcription	Brain Substantia Nigra	brain
48	chr15:51741600-51748800	Weak transcription	NHLF	lung
49	chr15:51742200-51746600	Weak transcription	Brain Germinal Matrix	brain
50	chr15:51742200-51747200	Weak transcription	Fetal Kidney	kidney

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