Variant report

Variant	nsv539527
Chromosome Location	chr8:20665835-20837761
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:245)
Chromatin interactive
region (count:13)
LncRNA
region (count:63)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:20708356-20708429	K562	blood:	n/a	n/a
2	ATF1	chr8:20809628-20809937	K562	blood:	n/a	n/a
3	BACH1	chr8:20813151-20813198	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr8:20836598-20836879	GM12878	blood:	n/a	n/a
5	CCNT2	chr8:20809452-20809864	K562	blood:	n/a	chr8:20809683-20809703
6	CEBPB	chr8:20676307-20676545	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr8:20748734-20748934	HepG2	liver:	n/a	chr8:20748823-20748834
8	CEBPB	chr8:20698511-20698684	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:20810677-20811262	IMR90	lung:	n/a	chr8:20811090-20811101
10	CEBPB	chr8:20795561-20795603	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:20768496-20768814	HepG2	liver:	n/a	chr8:20768654-20768665
12	CEBPB	chr8:20768508-20768763	K562	blood:	n/a	chr8:20768654-20768665
13	CEBPB	chr8:20768532-20768761	IMR90	lung:	n/a	chr8:20768654-20768665
14	CEBPB	chr8:20748795-20748932	A549	lung:	n/a	chr8:20748823-20748834
15	CEBPB	chr8:20809083-20809266	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:20768506-20768831	A549	lung:	n/a	chr8:20768654-20768665
17	CEBPB	chr8:20724123-20724465	IMR90	lung:	n/a	chr8:20724312-20724325
18	CEBPB	chr8:20810638-20811217	HepG2	liver:	n/a	chr8:20811090-20811101
19	CEBPB	chr8:20830191-20830296	H1-hESC	embryonic stem cell:	n/a	chr8:20830220-20830231
20	CEBPB	chr8:20699857-20700142	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:20723288-20723516	IMR90	lung:	n/a	n/a
22	CEBPB	chr8:20733261-20733461	HepG2	liver:	n/a	chr8:20733368-20733379
23	CEBPB	chr8:20698425-20698703	MCF-7	breast:	n/a	chr8:20698429-20698442
24	CEBPB	chr8:20810953-20811181	K562	blood:	n/a	chr8:20811090-20811101
25	CEBPB	chr8:20723345-20723491	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:20696250-20696463	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:20757415-20757431	A549	lung:	n/a	n/a
28	CEBPB	chr8:20810943-20811214	A549	lung:	n/a	chr8:20811090-20811101
29	CEBPB	chr8:20739346-20739560	HepG2	liver:	n/a	chr8:20739482-20739493
30	CEBPB	chr8:20830066-20830350	HepG2	liver:	n/a	chr8:20830220-20830231
31	CEBPD	chr8:20809552-20809922	K562	blood:	n/a	n/a
32	CEBPD	chr8:20809504-20809904	K562	blood:	n/a	n/a
33	CHD2	chr8:20676166-20676689	H1-hESC	embryonic stem cell:	n/a	chr8:20676510-20676520
34	CREB1	chr8:20676027-20676525	H1-hESC	embryonic stem cell:	n/a	chr8:20676281-20676294
35	CREB1	chr8:20676033-20676570	H1-hESC	embryonic stem cell:	n/a	chr8:20676281-20676294
36	CTCF	chr8:20792228-20792283	K562	blood:	n/a	n/a
37	CTCF	chr8:20746740-20746890	K562	blood:	n/a	n/a
38	CTCF	chr8:20790280-20790430	K562	blood:	n/a	chr8:20790367-20790388 chr8:20790365-20790383
39	CTCF	chr8:20693520-20693670	HCPEpiC	choroid plexus:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
40	CTCF	chr8:20693560-20693710	MCF-7	breast:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
41	CTCF	chr8:20693540-20693690	GM12864	blood:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
42	CTCF	chr8:20693493-20693764	GM12878	blood:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
43	CTCF	chr8:20693560-20693710	Caco-2	colon:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
44	CTCF	chr8:20693599-20693633	MCF-7	breast:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
45	CTCF	chr8:20693559-20693638	A549	lung:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
46	CTCF	chr8:20693473-20693741	K562	blood:	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	chr8:20693590-20693667	GM12878	blood:	n/a	chr8:20693611-20693632 chr8:20693609-20693627
49	CTCF	chr8:20753420-20753570	HepG2	liver:	n/a	n/a
50	CTCF	chr8:20790332-20790386	LNCaP	prostate:	n/a	chr8:20790365-20790383

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20674500-20674550	AG10803	skin:	n/a
2	chr8:20674500-20674550	AG10803	skin:	n/a
3	chr8:20725345-20725395	MCF-7	breast:	n/a
4	chr8:20674500-20674550	HNPCEpiC	eye:	n/a
5	chr8:20674500-20674550	HCPEpiC	choroid plexus:	n/a
6	chr8:20676367-20676417	MCF-7	breast:	n/a
7	chr8:20676367-20676417	Hela-S3	cervix:	n/a
8	chr8:20674500-20674550	PrEC	prostate:	n/a
9	chr8:20725345-20725395	CMK	blood:	n/a
10	chr8:20676123-20676173	HUVEC	blood vessel:	n/a
11	chr8:20676123-20676173	HCF	heart:	n/a
12	chr8:20676367-20676417	K562	blood:	n/a
13	chr8:20676367-20676417	HRE	kidney:	n/a
14	chr8:20676367-20676417	PANC-1	pancreas:	n/a
15	chr8:20676123-20676173	HIPEpiC	eye:	n/a
16	chr8:20676367-20676417	AG10803	skin:	n/a
17	chr8:20676367-20676417	SAEC	small airway:	n/a
18	chr8:20676123-20676173	HL-60	blood:	n/a
19	chr8:20676123-20676173	PANC-1	pancreas:	n/a
20	chr8:20725345-20725395	SAEC	small airway:	n/a
21	chr8:20725345-20725395	Hepatocyte	liver:	n/a
22	chr8:20674500-20674550	ovcar-3	ovarian:	n/a
23	chr8:20725345-20725395	H1-hESC	embryonic stem cell:	embryo
24	chr8:20674500-20674550	ECC-1	luminal epithelium:	n/a
25	chr8:20676123-20676173	H1-hESC	embryonic stem cell:	embryo
26	chr8:20676123-20676173	AG04450	lung:	fetal
27	chr8:20674500-20674550	SAEC	small airway:	n/a
28	chr8:20674500-20674550	HCM	heart:	n/a
29	chr8:20674500-20674550	Hela-S3	cervix:	n/a
30	chr8:20674500-20674550	GM12878	blood:	n/a
31	chr8:20676367-20676417	LNCaP	prostate:	n/a
32	chr8:20674500-20674550	T-47D	breast:	n/a
33	chr8:20725345-20725395	SKMC	muscle:	n/a
34	chr8:20674500-20674550	GM19239	blood:	n/a
35	chr8:20676367-20676417	AG09319	gingival:	n/a
36	chr8:20674500-20674550	Caco-2	colon:	n/a
37	chr8:20725345-20725395	PFSK-1	brain:	n/a
38	chr8:20676367-20676417	U87	brain:	n/a
39	chr8:20725345-20725395	AG09319	gingival:	n/a
40	chr8:20676123-20676173	Caco-2	colon:	n/a
41	chr8:20725345-20725395	HUVEC	blood vessel:	n/a
42	chr8:20725345-20725395	NH-A	brain:	n/a
43	chr8:20674500-20674550	NT2-D1	testis:	n/a
44	chr8:20674500-20674550	PANC-1	pancreas:	n/a
45	chr8:20676123-20676173	U87	brain:	n/a
46	chr8:20674500-20674550	H1-hESC	embryonic stem cell:	embryo
47	chr8:20674500-20674550	HCF	heart:	n/a
48	chr8:20725345-20725395	GM12892	blood:	n/a
49	chr8:20725345-20725395	HRCEpiC	kidney:	n/a
50	chr8:20676367-20676417	RPTEC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:20767548..20769104-chr8:20769526..20772463,2	MCF-7	breast:
2	chr8:20737626..20740045-chr8:20787296..20789914,2	K562	blood:
3	chr8:20767548..20769104-chr8:20769526..20772463,2	MCF-7	breast:
4	chr8:20781724..20783659-chr8:20784151..20785678,2	K562	blood:
5	chr8:20750920..20753775-chr8:20759115..20761137,3	K562	blood:
6	chr8:20781724..20783659-chr8:20784151..20785678,2	K562	blood:
7	chr8:20724387..20726387-chr8:20728763..20730962,2	K562	blood:
8	chr8:20737626..20740045-chr8:20787296..20789914,2	K562	blood:
9	chr8:20806761..20808497-chr8:20810222..20812992,2	K562	blood:
10	chr8:20724387..20726387-chr8:20728763..20730962,2	K562	blood:
11	chr8:20750920..20753775-chr8:20759115..20761137,3	K562	blood:
12	chr8:20831135..20833950-chr8:20835824..20837842,2	K562	blood:
13	chr20:55800391..55800924-chr8:20778716..20779696,2	MCF-7	breast:

(count:63 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1B2-4	chr8:20806210-20806304	ENSG00000254260
2	lnc-ATP6V1B2-5	chr8:20811523-20811586	ENSG00000254026
3	lnc-ATP6V1B2-5	chr8:20832315-20832531	NONHSAT125421
4	lnc-LZTS1-4	chr8:20791946-20792348	NONHSAT125404
5	lnc-ATP6V1B2-5	chr8:20826298-20826427	XLOC_006734
6	lnc-ATP6V1B2-5	chr8:20810638-20811007	ENSG00000253147
7	lnc-ATP6V1B2-5	chr8:20812165-20812283	NONHSAT125407
8	lnc-ATP6V1B2-5	chr8:20832315-20832533	XLOC_006734
9	lnc-ATP6V1B2-5	chr8:20811352-20811586	XLOC_006734
10	lnc-ATP6V1B2-5	chr8:20831497-20832164	XLOC_006734
11	lnc-ATP6V1B2-5	chr8:20831896-20832033	XLOC_006734
12	lnc-ATP6V1B2-5	chr8:20832315-20832540	ENSG00000253199
13	lnc-ATP6V1B2-5	chr8:20813195-20813631	NONHSAT125407
14	lnc-ATP6V1B2-5	chr8:20811153-20811204	ENSG00000253147
15	lnc-ATP6V1B2-5	chr8:20813196-20813631	XLOC_006734
16	lnc-LZTS1-2	chr8:20831244-20831388	ENSG00000254092
17	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
18	lnc-ATP6V1B2-5	chr8:20813196-20813345	ENSG00000253147
19	lnc-ATP6V1B2-5	chr8:20813196-20813346	XLOC_006734
20	lnc-LZTS1-2	chr8:20810159-20810427	XLOC_007018
21	lnc-ATP6V1B2-5	chr8:20813196-20813347	XLOC_006734
22	lnc-ATP6V1B2-5	chr8:20811352-20811586	ENSG00000253147
23	lnc-ATP6V1B2-5	chr8:20810025-20810427	NONHSAT125407
24	lnc-ATP6V1B2-5	chr8:20826298-20826482	NONHSAT125418
25	lnc-ATP6V1B2-5	chr8:20831913-20832033	NONHSAT125421
26	lnc-ATP6V1B2-5	chr8:20810937-20811204	XLOC_006734
27	lnc-ATP6V1B2-5	chr8:20811137-20811204	XLOC_006734
28	lnc-ATP6V1B2-5	chr8:20820292-20820412	XLOC_006734
29	lnc-ATP6V1B2-5	chr8:20831860-20832033	XLOC_006734
30	lnc-ATP6V1B2-5	chr8:20826298-20826415	ENSG00000253147
31	lnc-LZTS1-2	chr8:20810156-20810427	ENSG00000254092
32	lnc-LZTS1-2	chr8:20812166-20812283	XLOC_007018
33	lnc-LZTS1-2	chr8:20810905-20811014	XLOC_007018
34	lnc-ATP6V1B2-5	chr8:20831248-20831509	XLOC_006734
35	lnc-ATP6V1B2-4	chr8:20800453-20800763	ENSG00000254260
36	lnc-ATP6V1B2-5	chr8:20820292-20820412	ENSG00000254026
37	lnc-ATP6V1B2-5	chr8:20820076-20820412	NONHSAT125407
38	lnc-ATP6V1B2-5	chr8:20813196-20813345	ENSG00000253147
39	lnc-ATP6V1B2-5	chr8:20811352-20811586	XLOC_006734
40	lnc-ATP6V1B2-5	chr8:20811352-20811590	ENSG00000253147
41	lnc-LZTS1-2	chr8:20810159-20810427	XLOC_007018
42	lnc-ATP6V1B2-5	chr8:20820292-20820406	ENSG00000253147
43	lnc-ATP6V1B2-5	chr8:20812727-20812776	XLOC_006734
44	lnc-ATP6V1B2-5	chr8:20811351-20811590	NONHSAT125407
45	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
46	lnc-ATP6V1B2-5	chr8:20813196-20813347	XLOC_006734
47	lnc-ATP6V1B2-5	chr8:20820292-20820412	XLOC_006734
48	lnc-ATP6V1B2-5	chr8:20826298-20826830	XLOC_006734
49	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
50	lnc-ATP6V1B2-4	chr8:20798939-20799011	ENSG00000254260

No data

Variant related genes	Relation type
ENSG00000254260	TF binding region
TMEM97P2	TF binding region
ENSG00000254026	TF binding region
ENSG00000253147	TF binding region
ENSG00000253199	TF binding region
ENSG00000254092	TF binding region
ENSG00000254260	CpG island
TMEM97P2	CpG island
ENSG00000254026	CpG island
ENSG00000253147	CpG island
ENSG00000253199	CpG island
ENSG00000254092	CpG island
ENSG00000253147	chromatin interactions
ENSG00000254092	chromatin interactions
ENSG00000253199	chromatin interactions
ENSG00000254026	chromatin interactions
GRB2	miRNA target sites
HIF1AN	miRNA target sites
BMPR2	miRNA target sites
CAB39	miRNA target sites
LDLR	miRNA target sites
SCARB1	miRNA target sites
RAB14	miRNA target sites
TP53	miRNA target sites
SCD	miRNA target sites

Extended variants
information (count: 4970 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:4970 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36105710	chr8:20670800-20670801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545121933	chr8:20670840-20670841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553368244	chr8:20670876-20670877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76000830	chr8:20670898-20670899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530845982	chr8:20670919-20670920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114083073	chr8:20670920-20670921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187243504	chr8:20670934-20670935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557815851	chr8:20670947-20670948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192167181	chr8:20670958-20670959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368202443	chr8:20670959-20670960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539510855	chr8:20670973-20670974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185579966	chr8:20670982-20670983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569616574	chr8:20670989-20670990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536672622	chr8:20671034-20671035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555630052	chr8:20671053-20671054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573815629	chr8:20671076-20671077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540932482	chr8:20671082-20671083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2467527	chr8:20671096-20671097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs190502395	chr8:20671106-20671107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151113204	chr8:20671134-20671135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563471388	chr8:20671154-20671155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575029094	chr8:20671180-20671181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10711595	chr8:20671181-20671182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397891376	chr8:20671187-20671188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200172685	chr8:20671229-20671230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542697570	chr8:20671236-20671237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141521660	chr8:20671275-20671276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541500133	chr8:20671288-20671289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561342796	chr8:20671312-20671313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542137945	chr8:20671327-20671328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373178472	chr8:20671328-20671329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192667530	chr8:20671346-20671347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375963255	chr8:20671395-20671396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551477144	chr8:20671407-20671408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150239082	chr8:20671452-20671453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369279377	chr8:20671481-20671482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548656306	chr8:20671522-20671523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10107555	chr8:20671523-20671524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184513704	chr8:20671680-20671681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188663318	chr8:20671683-20671684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559868425	chr8:20671688-20671689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577395143	chr8:20671700-20671701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533391232	chr8:20671771-20671772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557419638	chr8:20671774-20671775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181085620	chr8:20671789-20671790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545381173	chr8:20671790-20671791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138909195	chr8:20671857-20671858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs60184909	chr8:20671892-20671893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543110072	chr8:20671896-20671897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369201216	chr8:20671930-20671931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20670800-20674200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:20671200-20671400	Enhancers	Right Ventricle	heart
3	chr8:20671400-20672800	Weak transcription	Right Ventricle	heart
4	chr8:20671600-20673000	Enhancers	Fetal Heart	heart
5	chr8:20672800-20673400	Enhancers	Right Ventricle	heart
6	chr8:20672800-20676000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr8:20673000-20673200	Enhancers	Gastric	stomach
8	chr8:20673000-20673800	Flanking Active TSS	Fetal Heart	heart
9	chr8:20673200-20676200	Weak transcription	Gastric	stomach
10	chr8:20673800-20674000	Enhancers	Fetal Heart	heart
11	chr8:20674200-20674400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr8:20674200-20674600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:20674400-20674600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:20674400-20675000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:20674600-20675800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr8:20674600-20677200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:20674800-20676200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr8:20675000-20675800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr8:20675200-20675400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr8:20675600-20676200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr8:20675800-20676000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr8:20675800-20676000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr8:20675800-20676000	Enhancers	Brain Germinal Matrix	brain
24	chr8:20675800-20676400	Enhancers	Placenta	Placenta
25	chr8:20675800-20679200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr8:20676000-20676200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:20676000-20676200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr8:20676000-20676200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:20676000-20676200	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr8:20676000-20676400	Enhancers	K562	blood
31	chr8:20676000-20676600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr8:20676000-20676800	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr8:20676000-20677600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:20676000-20678200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:20676000-20678400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr8:20676200-20676400	Enhancers	Gastric	stomach
37	chr8:20676200-20676600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr8:20676200-20676600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr8:20676200-20676600	Active TSS	Brain Germinal Matrix	brain
40	chr8:20676200-20676800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr8:20676200-20677000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr8:20676200-20677200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr8:20676200-20678400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr8:20676400-20676800	Weak transcription	Placenta	Placenta
45	chr8:20676400-20677000	Active TSS	Fetal Brain Female	brain
46	chr8:20676600-20677600	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr8:20676600-20677600	Enhancers	Fetal Brain Male	brain
48	chr8:20676600-20678400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:20676600-20678400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:20676600-20678400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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