Variant report

Variant	nsv1020160
Chromosome Location	chr8:20652610-20825810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:405)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:20809628-20809937	K562	blood:	n/a	n/a
2	ATF1	chr8:20708356-20708429	K562	blood:	n/a	n/a
3	BACH1	chr8:20813151-20813198	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:20660725-20660925	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr8:20809452-20809864	K562	blood:	n/a	chr8:20809683-20809703
6	CEBPB	chr8:20768506-20768831	A549	lung:	n/a	chr8:20768654-20768665
7	CEBPB	chr8:20810677-20811262	IMR90	lung:	n/a	chr8:20811090-20811101
8	CEBPB	chr8:20733261-20733461	HepG2	liver:	n/a	chr8:20733368-20733379
9	CEBPB	chr8:20757415-20757431	A549	lung:	n/a	n/a
10	CEBPB	chr8:20696250-20696463	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:20768496-20768814	HepG2	liver:	n/a	chr8:20768654-20768665
12	CEBPB	chr8:20723345-20723491	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:20748795-20748932	A549	lung:	n/a	chr8:20748823-20748834
14	CEBPB	chr8:20724123-20724465	IMR90	lung:	n/a	chr8:20724312-20724325
15	CEBPB	chr8:20699857-20700142	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:20748734-20748934	HepG2	liver:	n/a	chr8:20748823-20748834
17	CEBPB	chr8:20768508-20768763	K562	blood:	n/a	chr8:20768654-20768665
18	CEBPB	chr8:20768532-20768761	IMR90	lung:	n/a	chr8:20768654-20768665
19	CEBPB	chr8:20698425-20698703	MCF-7	breast:	n/a	chr8:20698429-20698442
20	CEBPB	chr8:20698511-20698684	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:20723288-20723516	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:20739346-20739560	HepG2	liver:	n/a	chr8:20739482-20739493
23	CEBPB	chr8:20810943-20811214	A549	lung:	n/a	chr8:20811090-20811101
24	CEBPB	chr8:20676307-20676545	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:20810953-20811181	K562	blood:	n/a	chr8:20811090-20811101
26	CEBPB	chr8:20809083-20809266	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:20795561-20795603	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:20810638-20811217	HepG2	liver:	n/a	chr8:20811090-20811101
29	CEBPD	chr8:20809552-20809922	K562	blood:	n/a	n/a
30	CEBPD	chr8:20809504-20809904	K562	blood:	n/a	n/a
31	CHD2	chr8:20676166-20676689	H1-hESC	embryonic stem cell:	n/a	chr8:20676510-20676520
32	CREB1	chr8:20676033-20676570	H1-hESC	embryonic stem cell:	n/a	chr8:20676281-20676294
33	CREB1	chr8:20676027-20676525	H1-hESC	embryonic stem cell:	n/a	chr8:20676281-20676294
34	CTCF	chr8:20790280-20790430	WERI-Rb-1	eye:	n/a	chr8:20790367-20790388 chr8:20790365-20790383
35	CTCF	chr8:20693559-20693638	A549	lung:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
36	CTCF	chr8:20720500-20720593	LNCaP	prostate:	n/a	n/a
37	CTCF	chr8:20790337-20790401	HepG2	liver:	n/a	chr8:20790367-20790388 chr8:20790365-20790383
38	CTCF	chr8:20753420-20753570	HepG2	liver:	n/a	n/a
39	CTCF	chr8:20693500-20693650	GM12872	blood:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
40	CTCF	chr8:20693594-20693666	Gliobla	brain:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
41	CTCF	chr8:20693541-20693679	K562	blood:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
42	CTCF	chr8:20803360-20803510	GM12865	blood:	n/a	n/a
43	CTCF	chr8:20693520-20693670	WERI-Rb-1	eye:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
44	CTCF	chr8:20693573-20693646	LNCaP	prostate:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
45	CTCF	chr8:20809940-20810090	HL-60	blood:	n/a	n/a
46	CTCF	chr8:20693454-20693797	H1-hESC	embryonic stem cell:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
47	CTCF	chr8:20693530-20693678	LNCaP	prostate:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
48	CTCF	chr8:20746760-20746910	Caco-2	colon:	n/a	n/a
49	CTCF	chr8:20693525-20693704	Kidney_OC	kidney:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
50	CTCF	chr8:20790260-20790410	HEK293	kidney:	n/a	chr8:20790367-20790388 chr8:20790365-20790383

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20674500-20674550	A549	lung:	n/a
2	chr8:20676123-20676173	ProgFib	skin:	n/a
3	chr8:20676123-20676173	SK-N-MC	brain:	n/a
4	chr8:20676123-20676173	Caco-2	colon:	n/a
5	chr8:20676367-20676417	HRE	kidney:	n/a
6	chr8:20674500-20674550	Jurkat	blood:	n/a
7	chr8:20725345-20725395	GM12891	blood:	n/a
8	chr8:20676123-20676173	HNPCEpiC	eye:	n/a
9	chr8:20676123-20676173	MCF10A-Er-Src	breast:	n/a
10	chr8:20725345-20725395	AG09319	gingival:	n/a
11	chr8:20725345-20725395	NB4	blood:	n/a
12	chr8:20674500-20674550	HepG2	liver:	n/a
13	chr8:20674500-20674550	ovcar-3	ovarian:	n/a
14	chr8:20725345-20725395	MCF-7	breast:	n/a
15	chr8:20676367-20676417	HAEpiC	amniotic membrane:	n/a
16	chr8:20725345-20725395	Jurkat	blood:	n/a
17	chr8:20676367-20676417	HEK293	kidney:	embryo
18	chr8:20674500-20674550	NT2-D1	testis:	n/a
19	chr8:20725345-20725395	HRE	kidney:	n/a
20	chr8:20725345-20725395	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:20676367-20676417	H1-hESC	embryonic stem cell:	embryo
22	chr8:20725345-20725395	GM12892	blood:	n/a
23	chr8:20676123-20676173	PrEC	prostate:	n/a
24	chr8:20676367-20676417	SK-N-SH_RA	brain:	n/a
25	chr8:20674500-20674550	SK-N-SH	brain:	n/a
26	chr8:20676123-20676173	HRPEpiC	eye:	n/a
27	chr8:20725345-20725395	SKMC	muscle:	n/a
28	chr8:20725345-20725395	HCPEpiC	choroid plexus:	n/a
29	chr8:20676123-20676173	ECC-1	luminal epithelium:	n/a
30	chr8:20725345-20725395	SK-N-SH	brain:	n/a
31	chr8:20725345-20725395	Hepatocyte	liver:	n/a
32	chr8:20676367-20676417	CMK	blood:	n/a
33	chr8:20725345-20725395	ProgFib	skin:	n/a
34	chr8:20725345-20725395	CMK	blood:	n/a
35	chr8:20676367-20676417	GM12891	blood:	n/a
36	chr8:20676367-20676417	GM12892	blood:	n/a
37	chr8:20676123-20676173	GM12892	blood:	n/a
38	chr8:20676123-20676173	HCF	heart:	n/a
39	chr8:20674500-20674550	HRPEpiC	eye:	n/a
40	chr8:20676123-20676173	HMEC	breast:	n/a
41	chr8:20676123-20676173	ovcar-3	ovarian:	n/a
42	chr8:20676123-20676173	AG09309	skin:	n/a
43	chr8:20676123-20676173	HCM	heart:	n/a
44	chr8:20725345-20725395	NT2-D1	testis:	n/a
45	chr8:20674500-20674550	HEK293	kidney:	embryo
46	chr8:20676367-20676417	HCF	heart:	n/a
47	chr8:20674500-20674550	SAEC	small airway:	n/a
48	chr8:20676367-20676417	HRCEpiC	kidney:	n/a
49	chr8:20676367-20676417	ECC-1	luminal epithelium:	n/a
50	chr8:20674500-20674550	HRE	kidney:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:20806761..20808497-chr8:20810222..20812992,2	K562	blood:
2	chr8:20781724..20783659-chr8:20784151..20785678,2	K562	blood:
3	chr8:20767548..20769104-chr8:20769526..20772463,2	MCF-7	breast:
4	chr8:20724387..20726387-chr8:20728763..20730962,2	K562	blood:
5	chr8:20750920..20753775-chr8:20759115..20761137,3	K562	blood:
6	chr8:20724387..20726387-chr8:20728763..20730962,2	K562	blood:
7	chr8:20781724..20783659-chr8:20784151..20785678,2	K562	blood:
8	chr8:20737626..20740045-chr8:20787296..20789914,2	K562	blood:
9	chr8:20767548..20769104-chr8:20769526..20772463,2	MCF-7	breast:
10	chr20:55800391..55800924-chr8:20778716..20779696,2	MCF-7	breast:
11	chr8:20750920..20753775-chr8:20759115..20761137,3	K562	blood:
12	chr8:20737626..20740045-chr8:20787296..20789914,2	K562	blood:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1B2-5	chr8:20813196-20813347	XLOC_006734
2	lnc-LZTS1-2	chr8:20810905-20811014	XLOC_007018
3	lnc-LZTS1-2	chr8:20810159-20810427	XLOC_007018
4	lnc-LZTS1-2	chr8:20810159-20810427	XLOC_007018
5	lnc-ATP6V1B2-5	chr8:20820292-20820406	ENSG00000253147
6	lnc-ATP6V1B2-5	chr8:20813196-20813345	ENSG00000253147
7	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
8	lnc-ATP6V1B2-5	chr8:20813196-20813346	XLOC_006734
9	lnc-ATP6V1B2-5	chr8:20811153-20811204	ENSG00000253147
10	lnc-ATP6V1B2-5	chr8:20820292-20820412	XLOC_006734
11	lnc-ATP6V1B2-5	chr8:20811352-20811590	XLOC_006734
12	lnc-ATP6V1B2-5	chr8:20813196-20813631	XLOC_006734
13	lnc-ATP6V1B2-4	chr8:20807598-20807686	ENSG00000254260
14	lnc-ATP6V1B2-5	chr8:20811137-20811204	XLOC_006734
15	lnc-ATP6V1B2-5	chr8:20810937-20811204	XLOC_006734
16	lnc-ATP6V1B2-5	chr8:20820144-20820412	NONHSAT125418
17	lnc-ATP6V1B2-5	chr8:20810025-20810427	NONHSAT125407
18	lnc-ATP6V1B2-5	chr8:20811352-20811586	XLOC_006734
19	lnc-ATP6V1B2-5	chr8:20813196-20813347	XLOC_006734
20	lnc-ATP6V1B2-4	chr8:20798939-20799011	ENSG00000254260
21	lnc-LZTS1-4	chr8:20791946-20792348	NONHSAT125404
22	lnc-ATP6V1B2-5	chr8:20812727-20812776	XLOC_006734
23	lnc-ATP6V1B2-5	chr8:20811352-20811586	ENSG00000253147
24	lnc-ATP6V1B2-5	chr8:20820292-20820412	ENSG00000254026
25	lnc-ATP6V1B2-5	chr8:20811352-20811586	XLOC_006734
26	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
27	lnc-ATP6V1B2-5	chr8:20820292-20820412	XLOC_006734
28	lnc-ATP6V1B2-5	chr8:20813385-20813631	ENSG00000254026
29	lnc-ATP6V1B2-5	chr8:20810638-20811204	NONHSAT125407
30	lnc-ATP6V1B2-5	chr8:20825695-20826830	NONHSAT125407
31	lnc-ATP6V1B2-5	chr8:20813196-20813345	ENSG00000253147
32	lnc-ATP6V1B2-5	chr8:20810638-20811007	ENSG00000253147
33	lnc-LZTS1-2	chr8:20810156-20810427	ENSG00000254092
34	lnc-ATP6V1B2-5	chr8:20813195-20813631	NONHSAT125407
35	lnc-ATP6V1B2-5	chr8:20812165-20812283	NONHSAT125407
36	lnc-ATP6V1B2-4	chr8:20800453-20800763	ENSG00000254260
37	lnc-ATP6V1B2-5	chr8:20820292-20820412	ENSG00000253147
38	lnc-ATP6V1B2-5	chr8:20820292-20820412	XLOC_006734
39	lnc-ATP6V1B2-5	chr8:20811352-20811590	ENSG00000253147
40	lnc-ATP6V1B2-5	chr8:20811523-20811586	ENSG00000254026
41	lnc-ATP6V1B2-5	chr8:20812726-20812776	NONHSAT125407
42	lnc-ATP6V1B2-4	chr8:20806210-20806304	ENSG00000254260
43	lnc-ATP6V1B2-5	chr8:20820076-20820412	NONHSAT125407
44	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
45	lnc-LZTS1-2	chr8:20812166-20812283	XLOC_007018
46	lnc-ATP6V1B2-5	chr8:20811351-20811590	NONHSAT125407

No data

Variant related genes	Relation type
ENSG00000254260	TF binding region
TMEM97P2	TF binding region
ENSG00000254026	TF binding region
ENSG00000253147	TF binding region
ENSG00000254260	CpG island
TMEM97P2	CpG island
ENSG00000254026	CpG island
ENSG00000253147	CpG island
ENSG00000253147	chromatin interactions
ENSG00000254026	chromatin interactions
SCD	miRNA target sites
LDLR	miRNA target sites
HIF1AN	miRNA target sites
SCARB1	miRNA target sites
GRB2	miRNA target sites
CAB39	miRNA target sites
RAB14	miRNA target sites

Extended variants
information (count: 4832 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:4832 , 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	rs558158461	chr8:20652610-20652611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576708074	chr8:20652663-20652664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143553618	chr8:20652719-20652720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147136079	chr8:20652738-20652739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574530485	chr8:20652765-20652766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541670954	chr8:20652818-20652819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374015398	chr8:20652820-20652821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560561475	chr8:20652836-20652837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572621457	chr8:20652837-20652838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370898894	chr8:20652852-20652853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572389776	chr8:20652875-20652876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74938246	chr8:20652919-20652920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528806949	chr8:20652926-20652927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531625813	chr8:20652929-20652930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544066379	chr8:20652937-20652938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140312660	chr8:20652961-20652962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184632986	chr8:20652968-20652969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376822692	chr8:20652969-20652970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540493200	chr8:20653108-20653109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188326513	chr8:20653118-20653119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529955116	chr8:20653132-20653133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192028650	chr8:20653170-20653171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73226021	chr8:20653219-20653220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143284252	chr8:20653238-20653239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144839696	chr8:20653252-20653253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548187069	chr8:20653254-20653255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553363653	chr8:20653258-20653259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570084006	chr8:20653260-20653261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537444650	chr8:20653275-20653276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556384478	chr8:20653278-20653279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189315353	chr8:20653319-20653320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113021317	chr8:20653337-20653338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554040458	chr8:20653365-20653366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148549016	chr8:20653373-20653374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532593791	chr8:20653388-20653389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558307068	chr8:20653414-20653415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182017687	chr8:20653426-20653427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10105275	chr8:20653439-20653440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185731200	chr8:20653562-20653563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs151102883	chr8:20653573-20653574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541211584	chr8:20653574-20653575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559483973	chr8:20653578-20653579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533367571	chr8:20653582-20653583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551806799	chr8:20653668-20653669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570465393	chr8:20653727-20653728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2410665	chr8:20653728-20653729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs549561428	chr8:20653730-20653731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115940998	chr8:20653737-20653738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535783755	chr8:20653780-20653781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563276814	chr8:20653806-20653807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20647400-20657600	Weak transcription	Fetal Heart	heart
2	chr8:20656400-20659400	Enhancers	Brain Germinal Matrix	brain
3	chr8:20656800-20657000	Enhancers	Fetal Brain Female	brain
4	chr8:20657000-20658200	Weak transcription	Fetal Brain Female	brain
5	chr8:20657200-20657400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:20657200-20658000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr8:20657200-20658400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:20657400-20658800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:20657400-20661000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr8:20657600-20658000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr8:20657600-20658000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:20657600-20658000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:20657600-20659400	Enhancers	Fetal Heart	heart
14	chr8:20657800-20658200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:20658000-20658200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:20658000-20659200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr8:20658000-20659400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr8:20658000-20661000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr8:20658200-20658600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:20658200-20658800	Enhancers	Fetal Brain Female	brain
21	chr8:20658200-20661000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr8:20658400-20659000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:20658600-20661400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:20659400-20659600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr8:20659400-20660200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:20659400-20660400	Weak transcription	Brain Germinal Matrix	brain
27	chr8:20659400-20661400	Weak transcription	Fetal Heart	heart
28	chr8:20660600-20660800	Enhancers	Brain Germinal Matrix	brain
29	chr8:20660600-20661200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr8:20661000-20661200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr8:20661000-20661400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:20661000-20661400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:20661400-20661800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:20661400-20662000	Enhancers	Fetal Heart	heart
35	chr8:20670800-20674200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:20671200-20671400	Enhancers	Right Ventricle	heart
37	chr8:20671400-20672800	Weak transcription	Right Ventricle	heart
38	chr8:20671600-20673000	Enhancers	Fetal Heart	heart
39	chr8:20672800-20673400	Enhancers	Right Ventricle	heart
40	chr8:20672800-20676000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr8:20673000-20673200	Enhancers	Gastric	stomach
42	chr8:20673000-20673800	Flanking Active TSS	Fetal Heart	heart
43	chr8:20673200-20676200	Weak transcription	Gastric	stomach
44	chr8:20673800-20674000	Enhancers	Fetal Heart	heart
45	chr8:20674200-20674400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr8:20674200-20674600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:20674400-20674600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr8:20674400-20675000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:20674600-20675800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr8:20674600-20677200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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