Variant report

Variant	nsv1019519
Chromosome Location	chr5:179866730-179959408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1765)
CpG islands
(count:1221)
Chromatin interactive
region (count:123)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1765 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179921098-179921441	K562	blood:	n/a	n/a
2	ARID3A	chr5:179920256-179920489	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:179942463-179942560	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:179921113-179921482	HepG2	liver:	n/a	n/a
5	ATF2	chr5:179921005-179921489	GM12878	blood:	n/a	n/a
6	BACH1	chr5:179897963-179898282	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:179928420-179928427	K562	blood:	n/a	n/a
8	BACH1	chr5:179921849-179922049	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr5:179920672-179920856	GM12878	blood:	n/a	n/a
10	BCL3	chr5:179894036-179894564	A549	lung:	n/a	chr5:179894213-179894222
11	BCL3	chr5:179954691-179955054	GM12878	blood:	n/a	n/a
12	BCL3	chr5:179920971-179921485	A549	lung:	n/a	chr5:179921385-179921398
13	BCL3	chr5:179920888-179921352	A549	lung:	n/a	n/a
14	BCL3	chr5:179868437-179868959	A549	lung:	n/a	n/a
15	BCL3	chr5:179954713-179954975	GM12878	blood:	n/a	n/a
16	BCL3	chr5:179896707-179896968	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:179920923-179921525	GM12878	blood:	n/a	chr5:179921385-179921398
18	BHLHE40	chr5:179921026-179921502	GM12878	blood:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
19	BHLHE40	chr5:179898034-179898300	K562	blood:	n/a	n/a
20	BHLHE40	chr5:179921021-179921760	HepG2	liver:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
21	BHLHE40	chr5:179891686-179891866	HepG2	liver:	n/a	n/a
22	BHLHE40	chr5:179921030-179921507	K562	blood:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
23	BHLHE40	chr5:179921070-179921448	A549	lung:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
24	BRCA1	chr5:179868488-179868947	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:179911356-179911715	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:179921108-179921449	HepG2	liver:	n/a	n/a
27	BRCA1	chr5:179921129-179921385	GM12878	blood:	n/a	n/a
28	BRCA1	chr5:179921084-179921414	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr5:179897962-179898279	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr5:179921080-179921450	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr5:179920966-179921464	K562	blood:	n/a	n/a
32	CBX3	chr5:179871650-179871951	K562	blood:	n/a	n/a
33	CBX3	chr5:179921050-179921324	K562	blood:	n/a	n/a
34	CCNT2	chr5:179921067-179922235	K562	blood:	n/a	chr5:179922219-179922228 chr5:179921246-179921255
35	CEBPB	chr5:179900102-179900150	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:179868693-179868804	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:179935301-179935425	Hela-S3	cervix:	n/a	chr5:179935367-179935378
38	CEBPB	chr5:179868558-179868900	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr5:179942299-179942558	HepG2	liver:	n/a	chr5:179942326-179942337
40	CEBPB	chr5:179935244-179935490	HepG2	liver:	n/a	chr5:179935367-179935378
41	CEBPB	chr5:179935285-179935444	A549	lung:	n/a	chr5:179935367-179935378
42	CEBPB	chr5:179868404-179869008	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:179868457-179868942	A549	lung:	n/a	n/a
44	CEBPB	chr5:179941917-179941926	K562	blood:	n/a	n/a
45	CEBPB	chr5:179923380-179923702	IMR90	lung:	n/a	chr5:179923545-179923556
46	CEBPB	chr5:179898000-179898320	Hela-S3	cervix:	n/a	chr5:179898175-179898188
47	CEBPB	chr5:179946221-179946350	A549	lung:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
48	CEBPB	chr5:179946180-179946318	Hela-S3	cervix:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
49	CEBPB	chr5:179921159-179921427	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:179890524-179890605	K562	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179958483-179958533	AoSMC	blood vessel:	n/a
2	chr5:179958483-179958533	AoSMC	blood vessel:	n/a
3	chr5:179921704-179921754	HCT-116	colon:	n/a
4	chr5:179886241-179886291	Hela-S3	cervix:	n/a
5	chr5:179921426-179921476	AG04450	lung:	fetal
6	chr5:179921349-179921399	HL-60	blood:	n/a
7	chr5:179921704-179921754	CMK	blood:	n/a
8	chr5:179921426-179921476	GM06990	blood:	n/a
9	chr5:179920202-179920252	GM19239	blood:	n/a
10	chr5:179921349-179921399	BE2_C	brain:	n/a
11	chr5:179886642-179886692	ovcar-3	ovarian:	n/a
12	chr5:179921670-179921720	HIPEpiC	eye:	n/a
13	chr5:179950726-179950776	ProgFib	skin:	n/a
14	chr5:179920202-179920252	ProgFib	skin:	n/a
15	chr5:179868587-179868637	SK-N-SH_RA	brain:	n/a
16	chr5:179921704-179921754	NH-A	brain:	n/a
17	chr5:179921704-179921754	AG04450	lung:	fetal
18	chr5:179918462-179918512	NHBE	bronchial:	n/a
19	chr5:179921286-179921336	AG04450	lung:	fetal
20	chr5:179921349-179921399	A549	lung:	n/a
21	chr5:179924999-179925049	PrEC	prostate:	n/a
22	chr5:179921426-179921476	BE2_C	brain:	n/a
23	chr5:179921655-179921705	ovcar-3	ovarian:	n/a
24	chr5:179920971-179921021	HNPCEpiC	eye:	n/a
25	chr5:179886642-179886692	HepG2	liver:	n/a
26	chr5:179924999-179925049	NT2-D1	testis:	n/a
27	chr5:179886241-179886291	AoSMC	blood vessel:	n/a
28	chr5:179922147-179922197	HCPEpiC	choroid plexus:	n/a
29	chr5:179943471-179943521	HCM	heart:	n/a
30	chr5:179921670-179921720	MCF-7	breast:	n/a
31	chr5:179924999-179925049	HAEpiC	amniotic membrane:	n/a
32	chr5:179921704-179921754	HL-60	blood:	n/a
33	chr5:179921349-179921399	GM19239	blood:	n/a
34	chr5:179950726-179950776	ECC-1	luminal epithelium:	n/a
35	chr5:179921704-179921754	HNPCEpiC	eye:	n/a
36	chr5:179924999-179925049	GM19239	blood:	n/a
37	chr5:179958313-179958363	Hela-S3	cervix:	n/a
38	chr5:179921349-179921399	GM12891	blood:	n/a
39	chr5:179922339-179922389	AoSMC	blood vessel:	n/a
40	chr5:179886241-179886291	HIPEpiC	eye:	n/a
41	chr5:179921286-179921336	A549	lung:	n/a
42	chr5:179950726-179950776	HCPEpiC	choroid plexus:	n/a
43	chr5:179921349-179921399	SK-N-SH	brain:	n/a
44	chr5:179921286-179921336	HRPEpiC	eye:	n/a
45	chr5:179922339-179922389	NB4	blood:	n/a
46	chr5:179921704-179921754	NHBE	bronchial:	n/a
47	chr5:179920202-179920252	RPTEC	kidney:	n/a
48	chr5:179921704-179921754	SK-N-SH_RA	brain:	n/a
49	chr5:179921349-179921399	MCF10A-Er-Src	breast:	n/a
50	chr5:179958313-179958363	ovcar-3	ovarian:	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:179922992..179929395-chr5:179931202..179936163,8	K562	blood:
2	chr5:179893921..179896183-chr5:179914785..179916976,2	MCF-7	breast:
3	chr5:179716783..179719079-chr5:179889653..179891805,2	MCF-7	breast:
4	chr5:179951729..179953788-chr5:179957919..179959696,2	MCF-7	breast:
5	chr5:179925282..179927939-chr5:180022784..180024577,2	K562	blood:
6	chr5:179892192..179893698-chr5:179898781..179900873,2	MCF-7	breast:
7	chr5:179937654..179940636-chr5:179942142..179944184,2	K562	blood:
8	chr5:179923677..179925323-chr5:179932980..179935315,2	MCF-7	breast:
9	chr5:179933515..179935509-chr5:179936709..179938826,2	K562	blood:
10	chr5:179720128..179721419-chr5:179897501..179899069,16	MCF-7	breast:
11	chr5:179926836..179929553-chr5:179936130..179939014,2	MCF-7	breast:
12	chr5:179777936..179782491-chr5:179891240..179895951,5	MCF-7	breast:
13	chr5:179935454..179937135-chr5:179951603..179954291,2	MCF-7	breast:
14	chr5:179933515..179935509-chr5:179936709..179938826,2	K562	blood:
15	chr5:179718171..179722134-chr5:179892968..179897954,8	MCF-7	breast:
16	chr5:179720972..179723069-chr5:179918796..179921248,2	MCF-7	breast:
17	chr5:179744163..179746642-chr5:179892937..179895669,2	MCF-7	breast:
18	chr5:179717189..179723869-chr5:179893101..179900893,11	MCF-7	breast:
19	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
20	chr5:179882912..179885325-chr5:179894280..179896586,2	MCF-7	breast:
21	chr5:179932250..179934206-chr5:179936886..179939142,2	MCF-7	breast:
22	chr5:179924830..179925800-chr7:65958004..65958762,2	NB4	blood:
23	chr5:179897206..179899731-chr5:179901883..179904757,4	K562	blood:
24	chr5:179929128..179931609-chr5:179936210..179937731,2	K562	blood:
25	chr5:179928367..179929867-chr8:141667673..141670357,2	MCF-7	breast:
26	chr5:179898756..179901287-chr5:179909042..179911505,2	MCF-7	breast:
27	chr5:179719269..179721828-chr5:179910236..179912739,3	MCF-7	breast:
28	chr5:179880821..179884780-chr5:179891609..179894265,3	MCF-7	breast:
29	chr5:179890341..179892861-chr5:179894283..179898100,3	MCF-7	breast:
30	chr5:179934009..179936437-chr5:179937326..179939535,2	K562	blood:
31	chr5:179899433..179901543-chr5:179921321..179923446,2	MCF-7	breast:
32	chr5:179756438..179759576-chr5:179909239..179913349,3	MCF-7	breast:
33	chr5:179885057..179887954-chr5:179889094..179891579,3	MCF-7	breast:
34	chr5:179910434..179912774-chr5:179917900..179919453,2	MCF-7	breast:
35	chr19:13263786..13264489-chr5:179894149..179895088,2	Hela-S3	cervix:
36	chr5:179913180..179915672-chr5:179919139..179922723,5	K562	blood:
37	chr5:179754405..179760149-chr5:179891592..179897254,9	MCF-7	breast:
38	chr5:179920138..179923580-chr5:179954774..179958751,3	MCF-7	breast:
39	chr5:179954302..179955834-chr5:179973302..179975583,2	K562	blood:
40	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
41	chr5:179923854..179927597-chr5:179974532..179977818,3	MCF-7	breast:
42	chr5:179890863..179893411-chr5:179896364..179898839,3	K562	blood:
43	chr22:19434914..19435485-chr5:179921372..179922106,2	Hela-S3	cervix:
44	chr5:179935454..179937135-chr5:179951603..179954291,2	MCF-7	breast:
45	chr5:179742474..179743351-chr5:179897684..179898604,3	MCF-7	breast:
46	chr5:179925134..179926691-chr5:179928454..179930583,2	K562	blood:
47	chr5:179944903..179947278-chr5:179974741..179976598,2	MCF-7	breast:
48	chr5:179778332..179781251-chr5:179920436..179923318,3	MCF-7	breast:
49	chr5:179932398..179934837-chr5:179942777..179944702,2	K562	blood:
50	chr19:47353550..47354350-chr5:179921157..179921678,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6-1	chr5:179894886-179895269	XLOC_004680
2	lnc-CNOT6-2	chr5:179868559-179868855	XLOC_004679
3	lnc-CNOT6-2	chr5:179869730-179870238	XLOC_004679
4	lnc-CNOT6-1	chr5:179910115-179910503	XLOC_004680

No data

Variant related genes	Relation type
CNOT6	TF binding region
RNU6-525P	TF binding region
ENSG00000250509	TF binding region
CNOT6	CpG island
RNU6-525P	CpG island
ENSG00000250509	CpG island
ENSG00000248367	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000042753	chromatin interactions
ENSG00000037280	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000242259	chromatin interactions
ENSG00000131459	chromatin interactions
ENSG00000113300	chromatin interactions
ENSG00000250509	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000185065	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000128829	chromatin interactions
ATXN1L	miRNA target sites
ATXN7	miRNA target sites

Extended variants
information (count: 3422 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3422 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2387193	chr5:179866730-179866731	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540313838	chr5:179866737-179866738	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs13161315	chr5:179866739-179866740	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs76650954	chr5:179866742-179866743	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs184427315	chr5:179866743-179866744	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs13161321	chr5:179866754-179866755	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs13180839	chr5:179866770-179866771	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149505771	chr5:179866817-179866818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573608473	chr5:179866864-179866865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7725643	chr5:179866880-179866881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552712105	chr5:179866892-179866893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372468865	chr5:179867058-179867059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148749049	chr5:179867061-179867062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545186012	chr5:179867099-179867100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565117615	chr5:179867109-179867110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575608494	chr5:179867165-179867166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs13185599	chr5:179867194-179867195	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs189015751	chr5:179867234-179867235	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs144670740	chr5:179867238-179867239	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs546699740	chr5:179867252-179867253	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs71613456	chr5:179867302-179867303	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs115248503	chr5:179867348-179867349	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs376548761	chr5:179867351-179867352	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs552343195	chr5:179867364-179867365	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs569153229	chr5:179867385-179867386	Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs538125809	chr5:179867455-179867456	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs548895587	chr5:179867458-179867459	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs532235658	chr5:179867474-179867475	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs552325279	chr5:179867498-179867499	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs537517822	chr5:179867500-179867501	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs181429454	chr5:179867502-179867503	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs112920119	chr5:179867517-179867518	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs76142578	chr5:179867530-179867531	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs60507193	chr5:179867535-179867536	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs552706690	chr5:179867537-179867538	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs572966603	chr5:179867569-179867570	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs185515256	chr5:179867577-179867578	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs558764927	chr5:179867588-179867589	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs575546680	chr5:179867609-179867610	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs544091433	chr5:179867615-179867616	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs561208783	chr5:179867621-179867622	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs574647513	chr5:179867644-179867645	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs191250863	chr5:179867662-179867663	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs370636349	chr5:179867724-179867725	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs147878437	chr5:179867752-179867753	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs181078548	chr5:179867761-179867762	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs532466089	chr5:179867797-179867798	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs12517962	chr5:179867841-179867842	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs562725404	chr5:179867855-179867856	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs368230119	chr5:179867882-179867883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179866000-179866800	ZNF genes & repeats	Spleen	Spleen
2	chr5:179866000-179869800	Enhancers	Placenta	Placenta
3	chr5:179866200-179867400	Enhancers	Pancreas	Pancrea
4	chr5:179866400-179868400	Enhancers	Hela-S3	cervix
5	chr5:179866600-179867200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:179866800-179867200	Weak transcription	Spleen	Spleen
7	chr5:179867200-179867400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr5:179867200-179867400	Flanking Bivalent TSS/Enh	NHEK	skin
9	chr5:179867200-179867600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:179867200-179867600	Enhancers	Esophagus	oesophagus
11	chr5:179867200-179867600	Enhancers	Spleen	Spleen
12	chr5:179867200-179867600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr5:179867200-179867800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:179867200-179868600	Enhancers	A549	lung
15	chr5:179867400-179867600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:179867400-179867600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:179867400-179867600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:179867400-179867600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
19	chr5:179867400-179867600	Bivalent Enhancer	NHEK	skin
20	chr5:179867400-179867800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:179867400-179867800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr5:179867400-179867800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr5:179867400-179868000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr5:179867400-179868000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:179867400-179868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr5:179867400-179868800	Weak transcription	Pancreas	Pancrea
27	chr5:179867600-179867800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:179867600-179868800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:179867600-179868800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:179867600-179869000	Enhancers	HepG2	liver
31	chr5:179868000-179868400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr5:179868400-179868800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr5:179868400-179869200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr5:179868400-179869200	Flanking Active TSS	Hela-S3	cervix
35	chr5:179868600-179869000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr5:179868600-179869000	Flanking Active TSS	A549	lung
37	chr5:179868600-179869200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:179868800-179869000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:179868800-179869000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr5:179868800-179869000	Enhancers	Pancreas	Pancrea
41	chr5:179868800-179869200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:179869000-179869200	Active TSS	A549	lung
43	chr5:179869000-179869200	Bivalent/Poised TSS	NHEK	skin
44	chr5:179869200-179869400	Enhancers	Hela-S3	cervix
45	chr5:179880800-179882400	Enhancers	Brain Germinal Matrix	brain
46	chr5:179881400-179881800	Enhancers	Fetal Brain Male	brain
47	chr5:179883400-179884200	Enhancers	GM12878-XiMat	blood
48	chr5:179883400-179884200	Enhancers	HepG2	liver
49	chr5:179885200-179885400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:179885200-179886000	Enhancers	Lung	lung

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