Variant report

Variant	nsv904284
Chromosome Location	chr15:62123600-62243197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:367)
Chromatin interactive
region (count:43)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:62171569-62171652	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:62199453-62200154	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:62180335-62180383	K562	blood:	n/a	n/a
4	ARID3A	chr15:62127748-62128097	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:62164169-62164478	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:62164156-62164420	K562	blood:	n/a	n/a
7	BACH1	chr15:62234203-62234206	K562	blood:	n/a	n/a
8	BATF	chr15:62132271-62132601	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:62126335-62126603	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:62127694-62128068	GM12878	blood:	n/a	chr15:62127863-62127879
11	BHLHE40	chr15:62127711-62128200	HepG2	liver:	n/a	chr15:62127863-62127879
12	BHLHE40	chr15:62126392-62126642	K562	blood:	n/a	n/a
13	BRCA1	chr15:62127807-62128021	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr15:62164191-62164533	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr15:62185381-62185684	K562	blood:	n/a	n/a
16	CEBPB	chr15:62225483-62225689	K562	blood:	n/a	chr15:62225584-62225597 chr15:62225586-62225597 chr15:62225531-62225544 chr15:62225584-62225597 chr15:62225584-62225597 chr15:62225586-62225597
17	CEBPB	chr15:62232985-62233209	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:62227701-62228189	K562	blood:	n/a	chr15:62227893-62227904
19	CEBPB	chr15:62239060-62239292	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:62180324-62180597	Hela-S3	cervix:	n/a	chr15:62180454-62180465
21	CEBPB	chr15:62123191-62123994	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr15:62197996-62198309	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:62227818-62228070	A549	lung:	n/a	chr15:62227893-62227904
24	CEBPB	chr15:62171161-62171355	HepG2	liver:	n/a	chr15:62171168-62171181
25	CEBPB	chr15:62180373-62180630	K562	blood:	n/a	chr15:62180454-62180465
26	CEBPB	chr15:62130645-62130664	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:62180336-62180636	A549	lung:	n/a	chr15:62180454-62180465
28	CEBPB	chr15:62180307-62180564	HepG2	liver:	n/a	chr15:62180454-62180465
29	CEBPB	chr15:62199668-62200070	HepG2	liver:	n/a	n/a
30	CEBPB	chr15:62123683-62123970	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr15:62180280-62180649	IMR90	lung:	n/a	chr15:62180454-62180465
32	CEBPB	chr15:62182374-62182601	A549	lung:	n/a	n/a
33	CEBPB	chr15:62123592-62124024	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr15:62180357-62180498	H1-hESC	embryonic stem cell:	n/a	chr15:62180454-62180465
35	CEBPB	chr15:62227747-62228056	Hela-S3	cervix:	n/a	chr15:62227893-62227904
36	CHD1	chr15:62163340-62163388	GM12878	blood:	n/a	n/a
37	CHD2	chr15:62221823-62221825	GM12878	blood:	n/a	n/a
38	CHD2	chr15:62126364-62126592	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr15:62127734-62128054	A549	lung:	n/a	n/a
40	CTCF	chr15:62164160-62164310	Caco-2	colon:	n/a	chr15:62164291-62164309
41	CTCF	chr15:62127766-62128014	Hela-S3	cervix:	n/a	chr15:62127876-62127892 chr15:62127877-62127890 chr15:62127875-62127893 chr15:62127880-62127888 chr15:62127870-62127891 chr15:62127877-62127890
42	CTCF	chr15:62126400-62126550	GM12867	blood:	n/a	chr15:62126470-62126488 chr15:62126465-62126486 chr15:62126472-62126485
43	CTCF	chr15:62164244-62164331	GM13976	blood:	n/a	chr15:62164293-62164314 chr15:62164291-62164309
44	CTCF	chr15:62126380-62126530	HL-60	blood:	n/a	chr15:62126470-62126488 chr15:62126465-62126486 chr15:62126472-62126485
45	CTCF	chr15:62164320-62164470	NB4	blood:	n/a	n/a
46	CTCF	chr15:62127800-62127950	GM12875	blood:	n/a	chr15:62127876-62127892 chr15:62127877-62127890 chr15:62127875-62127893 chr15:62127880-62127888 chr15:62127870-62127891 chr15:62127877-62127890
47	CTCF	chr15:62126440-62126590	GM12868	blood:	n/a	chr15:62126470-62126488 chr15:62126465-62126486 chr15:62126472-62126485
48	CTCF	chr15:62127398-62127437	GM19240	blood:	n/a	n/a
49	CTCF	chr15:62163940-62164090	GM12878	blood:	n/a	n/a
50	CTCF	chr15:62127561-62127603	GM12892	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:62126810-62126860	NHDF-neo	bronchial:	n/a
2	chr15:62126810-62126860	NHDF-neo	bronchial:	n/a
3	chr15:62126953-62127003	HL-60	blood:	n/a
4	chr15:62123648-62123698	AoSMC	blood vessel:	n/a
5	chr15:62123648-62123698	SK-N-MC	brain:	n/a
6	chr15:62126953-62127003	HNPCEpiC	eye:	n/a
7	chr15:62127170-62127220	AG09319	gingival:	n/a
8	chr15:62126810-62126860	HRPEpiC	eye:	n/a
9	chr15:62145960-62146010	GM12878	blood:	n/a
10	chr15:62140361-62140411	HCT-116	colon:	n/a
11	chr15:62145960-62146010	GM12892	blood:	n/a
12	chr15:62140361-62140411	HNPCEpiC	eye:	n/a
13	chr15:62123648-62123698	HIPEpiC	eye:	n/a
14	chr15:62145960-62146010	Jurkat	blood:	n/a
15	chr15:62126810-62126860	NB4	blood:	n/a
16	chr15:62127170-62127220	SAEC	small airway:	n/a
17	chr15:62140361-62140411	HMEC	breast:	n/a
18	chr15:62126953-62127003	A549	lung:	n/a
19	chr15:62126810-62126860	ECC-1	luminal epithelium:	n/a
20	chr15:62127170-62127220	PFSK-1	brain:	n/a
21	chr15:62126953-62127003	T-47D	breast:	n/a
22	chr15:62127170-62127220	HUVEC	blood vessel:	n/a
23	chr15:62145960-62146010	NB4	blood:	n/a
24	chr15:62126810-62126860	BJ	skin:	n/a
25	chr15:62145960-62146010	HMEC	breast:	n/a
26	chr15:62123648-62123698	PFSK-1	brain:	n/a
27	chr15:62140361-62140411	HCPEpiC	choroid plexus:	n/a
28	chr15:62145960-62146010	HRE	kidney:	n/a
29	chr15:62126810-62126860	HL-60	blood:	n/a
30	chr15:62126810-62126860	GM12878	blood:	n/a
31	chr15:62123648-62123698	SKMC	muscle:	n/a
32	chr15:62145960-62146010	U87	brain:	n/a
33	chr15:62140361-62140411	PFSK-1	brain:	n/a
34	chr15:62126953-62127003	HCF	heart:	n/a
35	chr15:62145960-62146010	SK-N-SH	brain:	n/a
36	chr15:62126953-62127003	NHBE	bronchial:	n/a
37	chr15:62126953-62127003	Jurkat	blood:	n/a
38	chr15:62126953-62127003	Caco-2	colon:	n/a
39	chr15:62145960-62146010	AG10803	skin:	n/a
40	chr15:62126810-62126860	HUVEC	blood vessel:	n/a
41	chr15:62140361-62140411	NH-A	brain:	n/a
42	chr15:62126953-62127003	HCPEpiC	choroid plexus:	n/a
43	chr15:62126810-62126860	GM06990	blood:	n/a
44	chr15:62140361-62140411	HCM	heart:	n/a
45	chr15:62145960-62146010	HIPEpiC	eye:	n/a
46	chr15:62145960-62146010	HRPEpiC	eye:	n/a
47	chr15:62145960-62146010	MCF-7	breast:	n/a
48	chr15:62126810-62126860	HRCEpiC	kidney:	n/a
49	chr15:62140361-62140411	Hela-S3	cervix:	n/a
50	chr15:62127170-62127220	SK-N-SH_RA	brain:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:62157514..62159480-chr15:62215874..62217523,2	K562	blood:
2	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
3	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
4	chr15:61994457..61995423-chr15:62125910..62126947,7	MCF-7	breast:
5	chr15:62148662..62150892-chr15:62154836..62157768,2	K562	blood:
6	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
7	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
8	chr15:62235589..62237658-chr15:62241156..62242944,2	K562	blood:
9	chr15:62178968..62180848-chr15:62186299..62188013,2	K562	blood:
10	chr15:62139945..62141808-chr15:62207864..62210759,2	K562	blood:
11	chr15:62164230..62164773-chr15:62363602..62364393,2	K562	blood:
12	chr15:62242750..62243662-chr5:173738637..173739199,2	MCF-7	breast:
13	chr15:62151269..62153840-chr15:62155833..62158326,2	K562	blood:
14	chr15:62213296..62215607-chr15:62227904..62230544,2	K562	blood:
15	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
16	chr15:62195135..62197262-chr15:62198825..62201096,2	MCF-7	breast:
17	chr15:60877823..60878717-chr15:62125845..62126508,2	MCF-7	breast:
18	chr15:62241235..62242799-chr15:62250211..62252735,2	K562	blood:
19	chr15:61994396..61995310-chr15:62127133..62128355,3	MCF-7	breast:
20	chr15:62223179..62225292-chr15:62226281..62228642,2	K562	blood:
21	chr15:62205557..62210722-chr15:62211814..62216434,5	K562	blood:
22	chr15:62231542..62233712-chr15:62238622..62240411,2	K562	blood:
23	chr15:62170697..62173317-chr15:62182241..62184749,2	MCF-7	breast:
24	chr15:62204266..62207135-chr15:62210768..62213468,2	MCF-7	breast:
25	chr15:61994526..61995351-chr15:62127496..62128239,2	MCF-7	breast:
26	chr15:61903995..61904705-chr15:62127271..62128182,2	K562	blood:
27	chr15:62160043..62163025-chr15:62359293..62361455,2	MCF-7	breast:
28	chr15:62195135..62197262-chr15:62198825..62201096,2	MCF-7	breast:
29	chr15:62222450..62224583-chr15:62247796..62249719,2	MCF-7	breast:
30	chr15:61993548..61996478-chr15:62124062..62125855,2	MCF-7	breast:
31	chr15:62151580..62153257-chr15:62155803..62158666,2	MCF-7	breast:
32	chr15:62178968..62180848-chr15:62186299..62188013,2	K562	blood:
33	chr15:61459279..61460193-chr15:62127417..62128076,3	K562	blood:
34	chr11:22957855..22958444-chr15:62239142..62239729,2	MCF-7	breast:
35	chr15:62170697..62173317-chr15:62182241..62184749,2	MCF-7	breast:
36	chr15:62142649..62144721-chr15:62150330..62151848,2	MCF-7	breast:
37	chr15:62236123..62237658-chr15:62241444..62244261,2	K562	blood:
38	chr15:61994504..61995651-chr15:62125875..62126906,5	MCF-7	breast:
39	chr15:62164211..62164737-chr15:62546261..62547255,2	K562	blood:
40	chr15:62114335..62116359-chr15:62122402..62125286,2	K562	blood:
41	chr15:62142649..62144721-chr15:62150330..62151848,2	MCF-7	breast:
42	chr15:62157514..62159480-chr15:62215874..62217523,2	K562	blood:
43	chr15:62148662..62150892-chr15:62154836..62157768,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2CD4A-2	chr15:62141163-62142028	NONHSAT044261
2	lnc-C2CD4A-12	chr15:62137441-62138449	NONHSAT044260
3	lnc-VPS13C-2	chr15:62126216-62126280	NONHSAT044258
4	lnc-VPS13C-2	chr15:62123916-62124203	FPKM1_group_10292_transcript_1
5	lnc-C2CD4A-2	chr15:62126951-62126976	ENSG00000259564.1
6	lnc-C2CD4A-2	chr15:62144055-62144351	ENSG00000259564.1
7	lnc-C2CD4A-10	chr15:62206624-62206875	NONHSAT044263
8	lnc-VPS13C-2	chr15:62123939-62124003	FPKM1_group_10292_transcript_1
9	lnc-C2CD4A-2	chr15:62141596-62141671	ENSG00000259564.1
10	lnc-VPS13C-2	chr15:62123916-62124203	NONHSAT044258

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	VPS13C	hsa-miR-128-3p	chr15:62145364-62145384
2	VPS13C	hsa-miR-26b-5p	chr15:62160105-62160099
3	VPS13C	hsa-miR-326	chr15:62145517-62145536
4	VPS13C	hsa-miR-186-5p	chr15:62160021-62160015
5	VPS13C	hsa-miR-186-5p	chr15:62160016-62160037
6	VPS13C	hsa-miR-26b-5p	chr15:62157423-62157416
7	VPS13C	hsa-miR-186-5p	chr15:62145406-62145427
8	VPS13C	hsa-miR-26b-5p	chr15:62160099-62160122
9	VPS13C	hsa-miR-128-3p	chr15:62160069-62160089

Variant related genes	Relation type
VPS13C	TF binding region
RN7SL613P	TF binding region
ENSG00000259564	TF binding region
VPS13C	CpG island
RN7SL613P	CpG island
ENSG00000259564	CpG island
ENSG00000264376	chromatin interactions
ENSG00000129003	chromatin interactions

Extended variants
information (count: 4829 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4829 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8036499	chr15:62123600-62123601	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566580683	chr15:62123607-62123608	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs78848457	chr15:62123610-62123611	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs558467300	chr15:62123618-62123619	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs570663419	chr15:62123626-62123627	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs369429207	chr15:62123634-62123635	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537730558	chr15:62123649-62123650	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs190116361	chr15:62123650-62123651	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs142801964	chr15:62123685-62123686	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs545565291	chr15:62123689-62123690	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs542629439	chr15:62123782-62123783	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs553130456	chr15:62123794-62123795	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs28405832	chr15:62123799-62123800	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs28485146	chr15:62123878-62123879	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs144214864	chr15:62123896-62123897	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs188464908	chr15:62123903-62123904	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs577401796	chr15:62123927-62123928	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs4316689	chr15:62123934-62123935	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs563189576	chr15:62123937-62123938	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs375352642	chr15:62123940-62123941	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs548209480	chr15:62123945-62123946	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs369043138	chr15:62123955-62123956	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs527384081	chr15:62123970-62123971	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs372495903	chr15:62124040-62124041	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs552280587	chr15:62124093-62124094	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs570535898	chr15:62124105-62124106	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs542483273	chr15:62124154-62124155	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs538069105	chr15:62124158-62124159	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs549632558	chr15:62124168-62124169	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs73428615	chr15:62124173-62124174	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536200019	chr15:62124180-62124181	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs531065310	chr15:62124199-62124200	Enhancers Weak transcription Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs554541721	chr15:62124206-62124207	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567106952	chr15:62124226-62124227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534020440	chr15:62124267-62124268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148382535	chr15:62124306-62124307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577331464	chr15:62124307-62124308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7177756	chr15:62124329-62124330	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs563127923	chr15:62124339-62124340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575204712	chr15:62124345-62124346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542583786	chr15:62124358-62124359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559874753	chr15:62124360-62124361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74749362	chr15:62124372-62124373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544913999	chr15:62124390-62124391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193145994	chr15:62124455-62124456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113132724	chr15:62124492-62124493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531366810	chr15:62124495-62124496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549571048	chr15:62124514-62124515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76089582	chr15:62124526-62124527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535354568	chr15:62124541-62124542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
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
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62121800-62126600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr15:62122400-62124200	Enhancers	Primary hematopoietic stem cells	blood
3	chr15:62122600-62123800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr15:62122600-62124200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr15:62122800-62123600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:62123000-62124000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr15:62123000-62124000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr15:62123000-62124200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:62123000-62124200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:62123000-62124400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr15:62123200-62123600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr15:62123200-62124000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
13	chr15:62123400-62123600	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr15:62123400-62123800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr15:62123400-62124000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr15:62123400-62124200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:62123400-62124200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr15:62123400-62124200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr15:62123400-62124400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr15:62123400-62124600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr15:62123400-62126400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr15:62123600-62123800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr15:62123600-62123800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr15:62123600-62124000	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr15:62123600-62124200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr15:62123600-62124200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr15:62124000-62124200	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr15:62124000-62126000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr15:62124200-62126600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr15:62124200-62127600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr15:62124200-62127600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr15:62126000-62126200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:62126000-62126400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr15:62126000-62126400	Enhancers	Spleen	Spleen
35	chr15:62126000-62128200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr15:62126000-62128200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:62126200-62126400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr15:62126200-62126400	Enhancers	Brain Substantia Nigra	brain
39	chr15:62126200-62126600	Enhancers	Primary B cells from peripheral blood	blood
40	chr15:62126200-62126800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr15:62126200-62126800	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr15:62126200-62126800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr15:62126200-62127000	Enhancers	Brain Cingulate Gyrus	brain
44	chr15:62126200-62127000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr15:62126200-62127800	Enhancers	Pancreas	Pancrea
46	chr15:62126200-62128200	Enhancers	Brain Anterior Caudate	brain
47	chr15:62126400-62126600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:62126400-62127000	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr15:62126400-62127200	Enhancers	Stomach Smooth Muscle	stomach
50	chr15:62126400-62127600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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