Variant report

Variant	esv19858
Chromosome Location	chr15:74911304-74925497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1274)
CpG islands
(count:366)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1274 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74913443-74913613	HepG2	liver:	n/a	n/a
2	ATF2	chr15:74913315-74913817	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr15:74913336-74913819	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr15:74913361-74913825	A549	lung:	n/a	n/a
5	ATF3	chr15:74913463-74913714	K562	blood:	n/a	n/a
6	BCL3	chr15:74922618-74922939	K562	blood:	n/a	n/a
7	BCL3	chr15:74918501-74919008	GM12878	blood:	n/a	n/a
8	BCL3	chr15:74918541-74918987	GM12878	blood:	n/a	n/a
9	BCL3	chr15:74922267-74923264	K562	blood:	n/a	n/a
10	BHLHE40	chr15:74923803-74924124	HepG2	liver:	n/a	n/a
11	BHLHE40	chr15:74924345-74924623	K562	blood:	n/a	n/a
12	BHLHE40	chr15:74919633-74919857	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:74922811-74923129	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:74913403-74913715	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:74913473-74913758	K562	blood:	n/a	n/a
16	BRCA1	chr15:74924306-74924616	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr15:74913529-74913709	HepG2	liver:	n/a	n/a
18	BRCA1	chr15:74913440-74913754	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr15:74923863-74923936	K562	blood:	n/a	n/a
20	CEBPB	chr15:74913379-74913726	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:74913436-74913711	K562	blood:	n/a	n/a
22	CEBPB	chr15:74923717-74924099	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:74923723-74924111	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:74913116-74913835	HepG2	liver:	n/a	n/a
25	CEBPB	chr15:74923659-74924046	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:74913358-74913849	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr15:74913407-74913676	K562	blood:	n/a	n/a
28	CHD2	chr15:74924387-74924532	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr15:74923836-74923939	K562	blood:	n/a	n/a
30	CHD2	chr15:74923979-74924037	HepG2	liver:	n/a	n/a
31	CHD2	chr15:74913519-74913827	GM12878	blood:	n/a	n/a
32	CHD2	chr15:74914250-74914557	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr15:74913390-74913775	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr15:74911883-74911941	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr15:74925096-74925098	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr15:74913461-74913597	HepG2	liver:	n/a	n/a
37	CHD2	chr15:74922529-74922705	K562	blood:	n/a	n/a
38	CHD2	chr15:74913429-74913790	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr15:74924396-74924658	A549	lung:	n/a	n/a
40	CREB1	chr15:74913336-74913872	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr15:74913418-74913759	A549	lung:	n/a	n/a
42	CTCF	chr15:74923290-74923383	LNCaP	prostate:	n/a	n/a
43	CTCF	chr15:74925220-74925370	AG09309	skin:	n/a	n/a
44	CTCF	chr15:74913432-74913781	LNCaP	prostate:	n/a	chr15:74913570-74913591 chr15:74913568-74913586 chr15:74913612-74913628
45	CTCF	chr15:74924346-74924617	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr15:74913355-74913822	GM12878	blood:	n/a	chr15:74913570-74913591 chr15:74913568-74913586 chr15:74913612-74913628
47	CTCF	chr15:74923980-74924130	AG09309	skin:	n/a	n/a
48	CTCF	chr15:74924400-74924550	GM12870	blood:	n/a	n/a
49	CTCF	chr15:74924420-74924570	HCM	heart:	n/a	n/a
50	CTCF	chr15:74923240-74923390	GM12874	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74914491-74914541	PFSK-1	brain:	n/a
2	chr15:74914491-74914541	SK-N-SH_RA	brain:	n/a
3	chr15:74914491-74914541	NB4	blood:	n/a
4	chr15:74914491-74914541	PrEC	prostate:	n/a
5	chr15:74912408-74912458	SK-N-SH_RA	brain:	n/a
6	chr15:74923934-74923984	AG04449	skin:	fetal
7	chr15:74914482-74914532	ovcar-3	ovarian:	n/a
8	chr15:74923934-74923984	Hepatocyte	liver:	n/a
9	chr15:74912408-74912458	H1-hESC	embryonic stem cell:	embryo
10	chr15:74923934-74923984	BJ	skin:	n/a
11	chr15:74914491-74914541	HRPEpiC	eye:	n/a
12	chr15:74912408-74912458	NH-A	brain:	n/a
13	chr15:74912474-74912524	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:74922293-74922343	SKMC	muscle:	n/a
15	chr15:74922293-74922343	PANC-1	pancreas:	n/a
16	chr15:74914482-74914532	HIPEpiC	eye:	n/a
17	chr15:74922293-74922343	SK-N-MC	brain:	n/a
18	chr15:74912474-74912524	HRCEpiC	kidney:	n/a
19	chr15:74922293-74922343	Jurkat	blood:	n/a
20	chr15:74912474-74912524	ProgFib	skin:	n/a
21	chr15:74914491-74914541	SAEC	small airway:	n/a
22	chr15:74923934-74923984	MCF-7	breast:	n/a
23	chr15:74912408-74912458	SK-N-MC	brain:	n/a
24	chr15:74922293-74922343	HCPEpiC	choroid plexus:	n/a
25	chr15:74914482-74914532	NH-A	brain:	n/a
26	chr15:74922293-74922343	HRPEpiC	eye:	n/a
27	chr15:74912408-74912458	ovcar-3	ovarian:	n/a
28	chr15:74914491-74914541	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:74914482-74914532	HepG2	liver:	n/a
30	chr15:74914491-74914541	HCM	heart:	n/a
31	chr15:74914482-74914532	NB4	blood:	n/a
32	chr15:74922293-74922343	AG04449	skin:	fetal
33	chr15:74914482-74914532	AG09309	skin:	n/a
34	chr15:74914491-74914541	HIPEpiC	eye:	n/a
35	chr15:74912474-74912524	BE2_C	brain:	n/a
36	chr15:74914482-74914532	A549	lung:	n/a
37	chr15:74914482-74914532	AG10803	skin:	n/a
38	chr15:74923934-74923984	T-47D	breast:	n/a
39	chr15:74922293-74922343	MCF10A-Er-Src	breast:	n/a
40	chr15:74914491-74914541	H1-hESC	embryonic stem cell:	embryo
41	chr15:74914482-74914532	T-47D	breast:	n/a
42	chr15:74914491-74914541	HL-60	blood:	n/a
43	chr15:74912408-74912458	SKMC	muscle:	n/a
44	chr15:74912408-74912458	Caco-2	colon:	n/a
45	chr15:74914491-74914541	RPTEC	kidney:	n/a
46	chr15:74912474-74912524	HAEpiC	amniotic membrane:	n/a
47	chr15:74914482-74914532	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:74914482-74914532	PrEC	prostate:	n/a
49	chr15:74912474-74912524	Caco-2	colon:	n/a
50	chr15:74912408-74912458	BE2_C	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74913467..74914497-chr15:74924158..74925086,3	MCF-7	breast:
2	chr15:74909966..74912107-chr15:74947107..74949319,2	K562	blood:
3	chr15:74665568..74668523-chr15:74922376..74925547,4	MCF-7	breast:
4	chr15:74923745..74927577-chr15:75051297..75054526,4	K562	blood:
5	chr15:74665743..74666548-chr15:74924006..74925016,4	MCF-7	breast:
6	chr15:74663970..74664961-chr15:74913133..74913678,2	MCF-7	breast:
7	chr15:74923393..74925278-chr15:75068761..75070889,2	MCF-7	breast:
8	chr15:74915721..74919302-chr15:75074662..75077539,3	MCF-7	breast:
9	chr15:74909806..74912416-chr15:75659270..75660874,2	MCF-7	breast:
10	chr15:74674778..74675397-chr15:74924008..74924955,2	K562	blood:
11	chr15:74924093..74925016-chr15:75060866..75061400,2	MCF-7	breast:
12	chr15:74921651..74924062-chr15:74933331..74936263,2	MCF-7	breast:
13	chr15:74923278..74925210-chr15:75067410..75069276,2	K562	blood:
14	chr15:74913200..74914026-chr15:74927109..74928135,3	MCF-7	breast:
15	chr15:74668556..74669508-chr15:74924452..74925052,2	K562	blood:
16	chr15:74666064..74666619-chr15:74924207..74924985,3	MCF-7	breast:
17	chr15:74911034..74913432-chr15:75186630..75189281,2	MCF-7	breast:
18	chr15:74923752..74925135-chr15:75060810..75061793,8	MCF-7	breast:
19	chr15:74917416..74920960-chr15:74922529..74925544,4	MCF-7	breast:
20	chr15:74924667..74926194-chr15:75061014..75063397,2	MCF-7	breast:
21	chr15:74666064..74667583-chr15:74922840..74924657,2	MCF-7	breast:
22	chr15:74922603..74925094-chr15:75061118..75062996,2	MCF-7	breast:
23	chr15:74913064..74914103-chr15:74922577..74924112,4	MCF-7	breast:
24	chr15:74665357..74666676-chr15:74923962..74924983,9	K562	blood:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	EDC3	hsa-miR-31-5p	chr15:74923705-74923726
2	EDC3	hsa-miR-31-5p	chr15:74924191-74924209
3	EDC3	hsa-miR-22-3p	chr15:74924661-74924685
4	EDC3	hsa-miR-22-3p	chr15:74924667-74924661

Variant related genes	Relation type
ENSG00000260919	TF binding region
CLK3	TF binding region
ENSG00000260919	CpG island
CLK3	CpG island
ENSG00000140400	chromatin interactions
ENSG00000178802	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000103653	chromatin interactions
ENSG00000179151	chromatin interactions
ENSG00000179335	chromatin interactions

Extended variants
information (count: 531 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569745588	chr15:74911313-74911314	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs59825838	chr15:74911346-74911347	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs58386058	chr15:74911357-74911358	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs111852558	chr15:74911372-74911373	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs148107950	chr15:74911375-74911376	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs141916549	chr15:74911440-74911441	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs552552363	chr15:74911454-74911455	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs574752275	chr15:74911459-74911460	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs542149566	chr15:74911462-74911463	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs545881555	chr15:74911474-74911475	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs370447220	chr15:74911515-74911516	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs193122515	chr15:74911526-74911527	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs377590393	chr15:74911528-74911529	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs574308834	chr15:74911559-74911560	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs575729159	chr15:74911575-74911576	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs150664892	chr15:74911579-74911580	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs200787328	chr15:74911587-74911588	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs148159573	chr15:74911593-74911594	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs573399106	chr15:74911620-74911621	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs199630534	chr15:74911627-74911628	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs562050993	chr15:74911647-74911648	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs142017053	chr15:74911648-74911649	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs150279637	chr15:74911653-74911654	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs542973892	chr15:74911668-74911669	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs183588535	chr15:74911680-74911681	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs28455057	chr15:74911707-74911708	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs200845851	chr15:74911711-74911712	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs199899941	chr15:74911724-74911725	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs570165554	chr15:74911788-74911789	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs565424437	chr15:74911876-74911877	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs113741589	chr15:74911896-74911897	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs562868343	chr15:74911927-74911928	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs534422449	chr15:74911988-74911989	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs6495118	chr15:74912012-74912013	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs559840260	chr15:74912038-74912039	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs567716066	chr15:74912116-74912117	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs535462249	chr15:74912125-74912126	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs118015157	chr15:74912128-74912129	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs575912192	chr15:74912142-74912143	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs142199523	chr15:74912167-74912168	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs558390454	chr15:74912207-74912208	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs573514601	chr15:74912242-74912243	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs540724440	chr15:74912247-74912248	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs530100240	chr15:74912293-74912294	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs573934140	chr15:74912305-74912306	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs11543198	chr15:74912328-74912329	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
47	rs147060953	chr15:74912346-74912347	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs371347609	chr15:74912350-74912351	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs371419854	chr15:74912367-74912368	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs373663118	chr15:74912368-74912369	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Autism	20531469	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74909000-74927000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:74909400-74911400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:74909400-74911600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr15:74909400-74911600	Weak transcription	Aorta	Aorta
5	chr15:74909400-74911600	Enhancers	Pancreas	Pancrea
6	chr15:74909400-74911800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr15:74909600-74911400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:74909600-74911400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr15:74909600-74911600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr15:74909600-74911600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr15:74909600-74911600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr15:74909600-74911800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:74909600-74912000	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr15:74909600-74913400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr15:74909800-74911400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr15:74909800-74911400	Enhancers	Liver	Liver
17	chr15:74909800-74911400	Enhancers	Brain Substantia Nigra	brain
18	chr15:74909800-74911400	Enhancers	Stomach Smooth Muscle	stomach
19	chr15:74909800-74911600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr15:74909800-74911600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr15:74909800-74911600	Enhancers	Left Ventricle	heart
22	chr15:74909800-74911800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:74909800-74912000	Genic enhancers	Fetal Intestine Small	intestine
24	chr15:74909800-74912000	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
25	chr15:74909800-74912000	Weak transcription	NH-A	brain
26	chr15:74909800-74912400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr15:74909800-74914000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr15:74909800-74914400	Weak transcription	HSMMtube	muscle
29	chr15:74910000-74911400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr15:74910000-74911400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr15:74910000-74911400	Enhancers	Fetal Heart	heart
32	chr15:74910000-74911600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr15:74910000-74911800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr15:74910000-74914000	Genic enhancers	Spleen	Spleen
35	chr15:74910000-74914400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
36	chr15:74910000-74917800	Strong transcription	Primary B cells from cord blood	blood
37	chr15:74910000-74931200	Strong transcription	NHLF	lung
38	chr15:74910000-74931600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr15:74910200-74911400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:74910200-74911400	Enhancers	Right Atrium	heart
41	chr15:74910200-74911600	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr15:74910200-74911600	Weak transcription	Osteobl	bone
43	chr15:74910200-74911800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr15:74910400-74911400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr15:74910400-74911600	Enhancers	HMEC	breast
46	chr15:74910400-74911800	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr15:74910400-74912000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr15:74910400-74913000	Strong transcription	NHEK	skin
49	chr15:74910400-74913800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr15:74910400-74913800	Genic enhancers	Colonic Mucosa	Colon

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