Variant report

Variant	nsv518316
Chromosome Location	chr15:74290993-74331083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:855)
Chromatin interactive
region (count:37)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr15:74299185-74299729	GM12878	blood:	n/a	n/a
2	BATF	chr15:74299367-74299722	GM12878	blood:	n/a	n/a
3	BCLAF1	chr15:74299291-74299801	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:74325395-74325601	K562	blood:	n/a	n/a
5	BHLHE40	chr15:74300303-74300683	GM12878	blood:	n/a	n/a
6	BRCA1	chr15:74303343-74303681	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr15:74303381-74303581	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:74303351-74303668	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr15:74301739-74301846	Hela-S3	cervix:	n/a	chr15:74301790-74301803
10	CEBPB	chr15:74303305-74303668	MCF-7	breast:	n/a	n/a
11	CEBPB	chr15:74329215-74329505	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr15:74302874-74303702	Hela-S3	cervix:	n/a	chr15:74302961-74302972
13	CEBPB	chr15:74302884-74303144	HepG2	liver:	n/a	chr15:74302961-74302972
14	CEBPB	chr15:74303328-74303633	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:74303337-74303532	K562	blood:	n/a	n/a
16	CEBPB	chr15:74315635-74315835	HepG2	liver:	n/a	chr15:74315727-74315738
17	CEBPB	chr15:74302828-74303123	IMR90	lung:	n/a	chr15:74302961-74302972
18	CHD1	chr15:74298930-74299247	GM12878	blood:	n/a	n/a
19	CHD2	chr15:74303325-74303580	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr15:74329262-74329541	MCF-7	breast:	n/a	chr15:74329390-74329408
21	CTCF	chr15:74329380-74329530	GM12864	blood:	n/a	chr15:74329390-74329408
22	CTCF	chr15:74329260-74329410	NHEK	skin:	n/a	chr15:74329390-74329408
23	CTCF	chr15:74329320-74329470	HRPEpiC	eye:	n/a	chr15:74329390-74329408
24	CTCF	chr15:74329340-74329490	HEEpiC	esophagus:	n/a	chr15:74329390-74329408
25	CTCF	chr15:74329304-74329451	ECC-1	luminal epithelium:	n/a	chr15:74329390-74329408
26	CTCF	chr15:74329340-74329490	HPAF	blood vessel:	n/a	chr15:74329390-74329408
27	CTCF	chr15:74329320-74329470	HMF	breast:	n/a	chr15:74329390-74329408
28	CTCF	chr15:74329280-74329430	GM12864	blood:	n/a	chr15:74329390-74329408
29	CTCF	chr15:74329340-74329490	SAEC	small airway:	n/a	chr15:74329390-74329408
30	CTCF	chr15:74329340-74329490	HCFaa	heart:	n/a	chr15:74329390-74329408
31	CTCF	chr15:74329320-74329470	GM12872	blood:	n/a	chr15:74329390-74329408
32	CTCF	chr15:74329291-74329515	Pancreas_OC	pancreas:	n/a	chr15:74329390-74329408
33	CTCF	chr15:74329300-74329450	AG04450	lung:	n/a	chr15:74329390-74329408
34	CTCF	chr15:74329269-74329545	MCF-7	breast:	n/a	chr15:74329390-74329408
35	CTCF	chr15:74329340-74329490	WERI-Rb-1	eye:	n/a	chr15:74329390-74329408
36	CTCF	chr15:74328680-74328830	HEEpiC	esophagus:	n/a	chr15:74328784-74328797
37	CTCF	chr15:74329215-74329568	K562	blood:	n/a	chr15:74329390-74329408
38	CTCF	chr15:74329780-74329930	HCM	heart:	n/a	n/a
39	CTCF	chr15:74329220-74329588	IMR90	lung:	n/a	chr15:74329390-74329408
40	CTCF	chr15:74329320-74329470	AG10803	skin:	n/a	chr15:74329390-74329408
41	CTCF	chr15:74329314-74329454	A549	lung:	n/a	chr15:74329390-74329408
42	CTCF	chr15:74329320-74329470	HPF	lung:	n/a	chr15:74329390-74329408
43	CTCF	chr15:74329340-74329490	HVMF	connective:	n/a	chr15:74329390-74329408
44	CTCF	chr15:74329040-74329817	A549	lung:	n/a	chr15:74329390-74329408
45	CTCF	chr15:74329340-74329490	MCF-7	breast:	n/a	chr15:74329390-74329408
46	CTCF	chr15:74329360-74329510	GM06990	blood:	n/a	chr15:74329390-74329408
47	CTCF	chr15:74329320-74329470	AG04450	lung:	n/a	chr15:74329390-74329408
48	CTCF	chr15:74329360-74329510	WERI-Rb-1	eye:	n/a	chr15:74329390-74329408
49	CTCF	chr15:74329320-74329470	HEEpiC	esophagus:	n/a	chr15:74329390-74329408
50	CTCF	chr15:74329340-74329490	HA-sp	spinal cord:	n/a	chr15:74329390-74329408

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74315539-74315589	NHDF-neo	bronchial:	n/a
2	chr15:74315539-74315589	NHDF-neo	bronchial:	n/a
3	chr15:74328425-74328475	NHDF-neo	bronchial:	n/a
4	chr15:74317780-74317830	ProgFib	skin:	n/a
5	chr15:74315539-74315589	HCM	heart:	n/a
6	chr15:74314816-74314866	U87	brain:	n/a
7	chr15:74317780-74317830	T-47D	breast:	n/a
8	chr15:74328425-74328475	MCF-7	breast:	n/a
9	chr15:74315474-74315524	HRE	kidney:	n/a
10	chr15:74291835-74291885	HMEC	breast:	n/a
11	chr15:74317259-74317309	HIPEpiC	eye:	n/a
12	chr15:74294468-74294518	NH-A	brain:	n/a
13	chr15:74315331-74315381	T-47D	breast:	n/a
14	chr15:74303043-74303093	SK-N-MC	brain:	n/a
15	chr15:74318422-74318472	AG04450	lung:	fetal
16	chr15:74303043-74303093	SK-N-SH_RA	brain:	n/a
17	chr15:74312279-74312329	GM12878	blood:	n/a
18	chr15:74317780-74317830	AG04450	lung:	fetal
19	chr15:74315179-74315229	SK-N-SH_RA	brain:	n/a
20	chr15:74318422-74318472	HCM	heart:	n/a
21	chr15:74318422-74318472	CMK	blood:	n/a
22	chr15:74317780-74317830	NB4	blood:	n/a
23	chr15:74315331-74315381	HAEpiC	amniotic membrane:	n/a
24	chr15:74315179-74315229	NHBE	bronchial:	n/a
25	chr15:74315539-74315589	HEK293	kidney:	embryo
26	chr15:74318422-74318472	SK-N-SH	brain:	n/a
27	chr15:74315539-74315589	SAEC	small airway:	n/a
28	chr15:74318422-74318472	SAEC	small airway:	n/a
29	chr15:74314816-74314866	RPTEC	kidney:	n/a
30	chr15:74312279-74312329	GM19239	blood:	n/a
31	chr15:74303043-74303093	HRCEpiC	kidney:	n/a
32	chr15:74317259-74317309	HCPEpiC	choroid plexus:	n/a
33	chr15:74315474-74315524	HRPEpiC	eye:	n/a
34	chr15:74317259-74317309	GM12878	blood:	n/a
35	chr15:74315331-74315381	Jurkat	blood:	n/a
36	chr15:74303043-74303093	HAEpiC	amniotic membrane:	n/a
37	chr15:74317259-74317309	GM06990	blood:	n/a
38	chr15:74315710-74315760	HNPCEpiC	eye:	n/a
39	chr15:74315539-74315589	SK-N-MC	brain:	n/a
40	chr15:74294468-74294518	GM12891	blood:	n/a
41	chr15:74315179-74315229	ovcar-3	ovarian:	n/a
42	chr15:74294468-74294518	Hepatocyte	liver:	n/a
43	chr15:74315474-74315524	SK-N-SH_RA	brain:	n/a
44	chr15:74315331-74315381	GM12891	blood:	n/a
45	chr15:74314816-74314866	BE2_C	brain:	n/a
46	chr15:74294468-74294518	ovcar-3	ovarian:	n/a
47	chr15:74317259-74317309	NHBE	bronchial:	n/a
48	chr15:74315474-74315524	ProgFib	skin:	n/a
49	chr15:74315474-74315524	HCPEpiC	choroid plexus:	n/a
50	chr15:74294468-74294518	GM12892	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74285465..74287394-chr15:74303680..74305234,2	MCF-7	breast:
2	chr15:74301606..74304928-chr15:74311289..74313632,4	MCF-7	breast:
3	chr15:74310869..74312553-chr15:74315639..74317174,2	MCF-7	breast:
4	chr15:74264988..74266186-chr15:74328671..74329935,19	MCF-7	breast:
5	chr15:74284477..74286185-chr15:74319336..74321648,2	MCF-7	breast:
6	chr15:74277595..74279838-chr15:74301921..74304643,3	MCF-7	breast:
7	chr15:74286840..74288514-chr15:74288531..74291100,2	MCF-7	breast:
8	chr15:74288636..74290848-chr15:74291772..74294059,2	MCF-7	breast:
9	chr15:74303068..74303808-chr15:74316250..74317180,2	MCF-7	breast:
10	chr15:74311100..74312963-chr15:74315126..74316880,2	MCF-7	breast:
11	chr15:74282696..74285036-chr15:74293067..74295399,2	MCF-7	breast:
12	chr15:74328869..74331984-chr15:74335288..74339582,4	MCF-7	breast:
13	chr15:74302863..74303504-chr15:74316793..74317518,2	MCF-7	breast:
14	chr15:74277650..74279742-chr15:74319526..74321446,2	MCF-7	breast:
15	chr15:74265011..74265899-chr15:74328914..74329841,6	MCF-7	breast:
16	chr15:74301606..74304928-chr15:74311289..74313632,4	MCF-7	breast:
17	chr15:74243215..74244120-chr15:74328879..74329879,2	MCF-7	breast:
18	chr15:74283960..74290618-chr15:74296413..74304371,10	MCF-7	breast:
19	chr15:74218748..74221720-chr15:74327759..74329413,2	MCF-7	breast:
20	chr15:74282640..74284615-chr15:74313984..74316844,2	MCF-7	breast:
21	chr15:74284526..74286693-chr15:74299037..74301704,2	MCF-7	breast:
22	chr15:74265025..74265814-chr15:74329334..74329841,2	K562	blood:
23	chr15:74330729..74333109-chr15:74334617..74337154,3	K562	blood:
24	chr15:74283820..74286284-chr15:74308005..74310945,2	MCF-7	breast:
25	chr15:74314012..74317004-chr15:74331925..74334688,2	K562	blood:
26	chr15:74176824..74179799-chr15:74328543..74330066,2	MCF-7	breast:
27	chr15:74299747..74301420-chr15:74301647..74303236,2	MCF-7	breast:
28	chr15:74264224..74266446-chr15:74328782..74330811,3	MCF-7	breast:
29	chr15:74310869..74312553-chr15:74315639..74317174,2	MCF-7	breast:
30	chr15:74284343..74287090-chr15:74322488..74325455,2	K562	blood:
31	chr15:74286453..74288589-chr15:74305603..74307209,2	MCF-7	breast:
32	chr15:74289396..74290975-chr15:74298748..74301175,2	K562	blood:
33	chr15:74276152..74278081-chr15:74290806..74293651,2	K562	blood:
34	chr15:74312798..74315530-chr15:74325452..74327125,2	K562	blood:
35	chr15:74299747..74301420-chr15:74301647..74303236,2	MCF-7	breast:
36	chr15:74303068..74303808-chr15:74316250..74317180,2	MCF-7	breast:
37	chr15:74285628..74288607-chr15:74300001..74303311,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISLR2-3	chr15:74325510-74325718	NONHSAT047196
2	lnc-ISLR2-3	chr15:74325497-74325546	NONHSAT047195
3	lnc-ISLR2-3	chr15:74324736-74325056	NONHSAT047195

No data

Variant related genes	Relation type
PML	TF binding region
STOML1	TF binding region
PML	CpG island
STOML1	CpG island
ENSG00000129038	chromatin interactions
ENSG00000261801	chromatin interactions
ENSG00000067221	chromatin interactions
ENSG00000140464	chromatin interactions

Extended variants
information (count: 1405 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3784563	chr15:74290993-74290994	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537792968	chr15:74291000-74291001	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs3784562	chr15:74291023-74291024	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs571327630	chr15:74291033-74291034	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs181946098	chr15:74291045-74291046	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs78189619	chr15:74291105-74291106	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs111617563	chr15:74291132-74291133	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs561468373	chr15:74291209-74291210	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs3784561	chr15:74291239-74291240	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs3784560	chr15:74291244-74291245	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs576339255	chr15:74291262-74291263	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs77973063	chr15:74291313-74291314	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs75263225	chr15:74291323-74291324	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184766472	chr15:74291359-74291360	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs76321828	chr15:74291387-74291388	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543209713	chr15:74291518-74291519	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs548013402	chr15:74291541-74291542	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532451541	chr15:74291564-74291565	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs563168427	chr15:74291567-74291568	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs541551479	chr15:74291601-74291602	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560081655	chr15:74291654-74291655	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs149004276	chr15:74291655-74291656	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs548906463	chr15:74291662-74291663	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs547438294	chr15:74291689-74291690	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs143836797	chr15:74291705-74291706	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs34403114	chr15:74291744-74291745	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11635930	chr15:74291751-74291752	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549775499	chr15:74291778-74291779	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs571290876	chr15:74291800-74291801	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs79862065	chr15:74291891-74291892	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs565509571	chr15:74291897-74291898	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs537507746	chr15:74291931-74291932	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs137869131	chr15:74291948-74291949	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11636016	chr15:74291976-74291977	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs147894664	chr15:74292035-74292036	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs114078857	chr15:74292095-74292096	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541295384	chr15:74292137-74292138	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs576300680	chr15:74292165-74292166	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs74417967	chr15:74292173-74292174	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368015472	chr15:74292176-74292177	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75253291	chr15:74292194-74292195	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188367512	chr15:74292200-74292201	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140818472	chr15:74292236-74292237	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180780742	chr15:74292245-74292246	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186706548	chr15:74292278-74292279	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559750648	chr15:74292285-74292286	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574843409	chr15:74292295-74292296	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114452946	chr15:74292368-74292369	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537193646	chr15:74292369-74292370	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556773378	chr15:74292378-74292379	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1824 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74288200-74291000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr15:74288200-74301800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr15:74288200-74303000	Weak transcription	A549	lung
4	chr15:74288200-74303800	Weak transcription	Brain Angular Gyrus	brain
5	chr15:74288200-74331000	Weak transcription	Fetal Heart	heart
6	chr15:74289600-74302400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr15:74289800-74291400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr15:74289800-74291600	Weak transcription	Fetal Brain Male	brain
9	chr15:74289800-74292000	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr15:74289800-74292000	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
11	chr15:74289800-74293000	Genic enhancers	Primary T cells fromperipheralblood	blood
12	chr15:74289800-74296000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
13	chr15:74289800-74303200	Weak transcription	Brain Substantia Nigra	brain
14	chr15:74289800-74331000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr15:74290000-74291000	Genic enhancers	Fetal Muscle Leg	muscle
16	chr15:74290000-74291000	Genic enhancers	Sigmoid Colon	Sigmoid Colon
17	chr15:74290000-74291200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr15:74290000-74291200	Enhancers	Right Atrium	heart
19	chr15:74290000-74291200	Genic enhancers	Spleen	Spleen
20	chr15:74290000-74291400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
21	chr15:74290000-74291400	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr15:74290000-74291600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr15:74290000-74291600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
24	chr15:74290000-74292000	Genic enhancers	Primary T cells from cord blood	blood
25	chr15:74290000-74292000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr15:74290000-74295200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr15:74290000-74299000	Weak transcription	Stomach Mucosa	stomach
28	chr15:74290000-74303400	Weak transcription	Fetal Kidney	kidney
29	chr15:74290000-74314800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:74290200-74291000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:74290200-74291000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:74290200-74291000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:74290200-74291000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr15:74290200-74291000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr15:74290200-74291000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:74290200-74291000	Weak transcription	Colon Smooth Muscle	Colon
37	chr15:74290200-74291000	Strong transcription	Fetal Intestine Small	intestine
38	chr15:74290200-74291000	Genic enhancers	Placenta	Placenta
39	chr15:74290200-74291000	Genic enhancers	Gastric	stomach
40	chr15:74290200-74291000	Genic enhancers	Lung	lung
41	chr15:74290200-74291000	Genic enhancers	Right Ventricle	heart
42	chr15:74290200-74291200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:74290200-74291200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr15:74290200-74291400	Strong transcription	Placenta Amnion	Placenta Amnion
45	chr15:74290200-74291600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr15:74290200-74291600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr15:74290200-74292000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr15:74290200-74292000	Genic enhancers	Primary B cells from cord blood	blood
49	chr15:74290200-74292000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:74290200-74292000	Strong transcription	Cortex derived primary cultured neurospheres	brain

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