Variant report

Variant	nsv898759
Chromosome Location	chr12:10454556-10583365
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2124)
CpG islands
(count:1223)
Chromatin interactive
region (count:38)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2124 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
2	ARID3A	chr12:10513720-10513857	K562	blood:	n/a	n/a
3	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
5	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:10536954-10536986	K562	blood:	n/a	n/a
7	ARID3A	chr12:10548121-10548681	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
10	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
11	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
12	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
13	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
14	ATF2	chr12:10470709-10471203	GM12878	blood:	n/a	n/a
15	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:10456577-10457005	GM12878	blood:	n/a	n/a
17	ATF2	chr12:10544776-10545621	GM12878	blood:	n/a	n/a
18	ATF2	chr12:10470741-10471136	GM12878	blood:	n/a	n/a
19	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
20	ATF2	chr12:10473155-10473759	GM12878	blood:	n/a	n/a
21	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
23	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
24	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
25	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
26	ATF3	chr12:10515933-10516347	K562	blood:	n/a	n/a
27	BACH1	chr12:10517085-10517124	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
29	BATF	chr12:10456621-10457029	GM12878	blood:	n/a	n/a
30	BATF	chr12:10516901-10517786	GM12878	blood:	n/a	n/a
31	BATF	chr12:10470851-10471221	GM12878	blood:	n/a	chr12:10471022-10471030
32	BATF	chr12:10473160-10473741	GM12878	blood:	n/a	n/a
33	BATF	chr12:10455627-10455902	GM12878	blood:	n/a	chr12:10455749-10455760
34	BATF	chr12:10473434-10473653	GM12878	blood:	n/a	n/a
35	BATF	chr12:10473216-10473419	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:10547875-10548349	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:10516986-10517620	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:10473293-10473615	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:10547793-10548282	GM12878	blood:	n/a	n/a
40	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
41	BCL11A	chr12:10544909-10545281	GM12878	blood:	n/a	n/a
42	BCL11A	chr12:10515491-10515913	GM12878	blood:	n/a	n/a
43	BCL11A	chr12:10517007-10517370	GM12878	blood:	n/a	n/a
44	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a
45	BCL3	chr12:10515498-10515948	GM12878	blood:	n/a	n/a
46	BCL3	chr12:10456668-10457144	GM12878	blood:	n/a	n/a
47	BCL3	chr12:10470815-10471173	GM12878	blood:	n/a	chr12:10470997-10471006
48	BCLAF1	chr12:10473313-10473710	GM12878	blood:	n/a	n/a
49	BCLAF1	chr12:10516769-10517765	GM12878	blood:	n/a	n/a
50	BCLAF1	chr12:10544894-10545448	GM12878	blood:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10460612-10460662	HCM	heart:	n/a
2	chr12:10544636-10544686	IMR90	lung:	fetal
3	chr12:10455788-10455838	T-47D	breast:	n/a
4	chr12:10460612-10460662	HCM	heart:	n/a
5	chr12:10544636-10544686	IMR90	lung:	fetal
6	chr12:10455788-10455838	T-47D	breast:	n/a
7	chr12:10459923-10459973	U87	brain:	n/a
8	chr12:10460639-10460689	RPTEC	kidney:	n/a
9	chr12:10465272-10465322	AG09309	skin:	n/a
10	chr12:10456885-10456935	A549	lung:	n/a
11	chr12:10544636-10544686	MCF10A-Er-Src	breast:	n/a
12	chr12:10459912-10459962	NH-A	brain:	n/a
13	chr12:10469147-10469197	NHDF-neo	bronchial:	n/a
14	chr12:10583355-10583405	GM19239	blood:	n/a
15	chr12:10459972-10460022	SK-N-SH	brain:	n/a
16	chr12:10525233-10525283	BE2_C	brain:	n/a
17	chr12:10532046-10532096	H1-hESC	embryonic stem cell:	embryo
18	chr12:10560602-10560652	T-47D	breast:	n/a
19	chr12:10544636-10544686	T-47D	breast:	n/a
20	chr12:10570179-10570229	HCF	heart:	n/a
21	chr12:10525233-10525283	AG04450	lung:	fetal
22	chr12:10544636-10544686	NHDF-neo	bronchial:	n/a
23	chr12:10543073-10543123	ProgFib	skin:	n/a
24	chr12:10459923-10459973	MCF10A-Er-Src	breast:	n/a
25	chr12:10515574-10515624	HepG2	liver:	n/a
26	chr12:10459972-10460022	SAEC	small airway:	n/a
27	chr12:10515091-10515141	Caco-2	colon:	n/a
28	chr12:10459972-10460022	H1-hESC	embryonic stem cell:	embryo
29	chr12:10583355-10583405	H1-hESC	embryonic stem cell:	embryo
30	chr12:10460639-10460689	HRPEpiC	eye:	n/a
31	chr12:10460639-10460689	HCPEpiC	choroid plexus:	n/a
32	chr12:10543073-10543123	Hela-S3	cervix:	n/a
33	chr12:10532046-10532096	IMR90	lung:	fetal
34	chr12:10560602-10560652	AG09309	skin:	n/a
35	chr12:10583355-10583405	NB4	blood:	n/a
36	chr12:10515091-10515141	BE2_C	brain:	n/a
37	chr12:10543073-10543123	HNPCEpiC	eye:	n/a
38	chr12:10460612-10460662	T-47D	breast:	n/a
39	chr12:10469147-10469197	K562	blood:	n/a
40	chr12:10459923-10459973	AG04449	skin:	fetal
41	chr12:10543073-10543123	MCF10A-Er-Src	breast:	n/a
42	chr12:10455788-10455838	NHDF-neo	bronchial:	n/a
43	chr12:10460612-10460662	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:10543073-10543123	HCF	heart:	n/a
46	chr12:10583355-10583405	HRCEpiC	kidney:	n/a
47	chr12:10570179-10570229	GM12892	blood:	n/a
48	chr12:10465272-10465322	A549	lung:	n/a
49	chr12:10570179-10570229	PANC-1	pancreas:	n/a
50	chr12:10560602-10560652	GM12892	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10483978..10484906-chr12:10714545..10715159,3	MCF-7	breast:
2	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
3	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
4	chr12:10484518..10485026-chr12:10826902..10827419,2	MCF-7	breast:
5	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
6	chr12:10506746..10508549-chr12:10514255..10516412,2	K562	blood:
7	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
8	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
9	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
10	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
11	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
12	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
13	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
14	chr12:10484044..10484911-chr12:10711156..10712037,3	MCF-7	breast:
15	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
16	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
17	chr12:10515701..10517485-chr12:10526352..10529351,3	K562	blood:
18	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
19	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
20	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
21	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
22	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
23	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
24	chr12:10484385..10484963-chr12:10714626..10715246,2	MCF-7	breast:
25	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
26	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
27	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
28	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
29	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:
30	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
31	chr12:10528733..10530247-chr12:10762165..10764402,2	K562	blood:
32	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
33	chr12:10453243..10455277-chr12:10460503..10462364,2	K562	blood:
34	chr12:10483953..10484953-chr12:10826469..10827411,2	K562	blood:
35	chr12:10515701..10519228-chr12:10526352..10529377,4	K562	blood:
36	chr12:10484283..10485072-chr12:10714510..10715568,4	K562	blood:
37	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
38	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155
2	lnc-KLRD1-1	chr12:10526634-10526735	ENSG00000245648
3	lnc-GABARAPL1-3	chr12:10464063-10464214	NONHSAT026875
4	lnc-RP11-277P12.7.1-2	chr12:10488711-10488908	ENSG00000256288
5	lnc-GABARAPL1-3	chr12:10460544-10460683	NONHSAT026878
6	lnc-GABARAPL1-3	chr12:10457065-10457146	NONHSAT026875
7	lnc-RP11-277P12.7.1-2	chr12:10485460-10485662	ENSG00000256288
8	lnc-GABARAPL1-3	chr12:10462225-10462287	NONHSAT026878
9	lnc-GABARAPL1-3	chr12:10460577-10462287	NONHSAT026875
10	lnc-RP11-277P12.7.1-2	chr12:10490644-10490891	ENSG00000256288
11	lnc-GABARAPL1-3	chr12:10467272-10467608	NONHSAT026875
12	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648
13	lnc-GABARAPL1-3	chr12:10464063-10464282	NONHSAT026878
14	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
15	lnc-GABARAPL1-3	chr12:10466009-10466112	NONHSAT026875
16	lnc-KLRD1-1	chr12:10548778-10551105	ENSG00000245648
17	lnc-KLRD1-1	chr12:10532301-10532435	ENSG00000245648

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLRK1	hsa-miR-9-5p	chr12:10525600-10525624

Variant related genes	Relation type
ENSG00000256288	TF binding region
KLRC3	TF binding region
KLRK1	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000256155	TF binding region
ENSG00000245648	TF binding region
KLRD1	TF binding region
ENSG00000256288	CpG island
KLRC3	CpG island
KLRK1	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000256155	CpG island
ENSG00000245648	CpG island
KLRD1	CpG island
ENSG00000123728	chromatin interactions
ENSG00000256888	chromatin interactions
ENSG00000213809	chromatin interactions
ENSG00000060140	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000205809	chromatin interactions
ENSG00000134539	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000255641	chromatin interactions
ESR1	miRNA target sites
NFIB	miRNA target sites
SMAD4	miRNA target sites
LPHN2	miRNA target sites
KIAA1967	miRNA target sites
RNF111	miRNA target sites

Extended variants
information (count: 5540 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5540 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3912117	chr12:10454556-10454557	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79540786	chr12:10454585-10454586	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs559644644	chr12:10454587-10454588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs71450036	chr12:10454604-10454605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76880735	chr12:10454612-10454613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7136409	chr12:10454737-10454738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs558372347	chr12:10454746-10454747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561970456	chr12:10454750-10454751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562904752	chr12:10454756-10454757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs117618150	chr12:10454777-10454778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191432948	chr12:10454807-10454808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182988313	chr12:10454840-10454841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537693509	chr12:10454845-10454846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187288631	chr12:10454869-10454870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12824509	chr12:10454895-10454896	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566409772	chr12:10454912-10454913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546782692	chr12:10454936-10454937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs78440293	chr12:10454979-10454980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529201152	chr12:10454983-10454984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549258071	chr12:10455019-10455020	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7297895	chr12:10455026-10455027	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557708028	chr12:10455030-10455031	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573944031	chr12:10455049-10455050	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370780801	chr12:10455054-10455055	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7308601	chr12:10455055-10455056	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs146094724	chr12:10455094-10455095	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs11838090	chr12:10455134-10455135	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs79677300	chr12:10455153-10455154	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs573365162	chr12:10455196-10455197	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191777338	chr12:10455213-10455214	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182463325	chr12:10455227-10455228	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543810700	chr12:10455236-10455237	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs10772255	chr12:10455250-10455251	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs75750914	chr12:10455285-10455286	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs533499696	chr12:10455286-10455287	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs139743275	chr12:10455304-10455305	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs115755751	chr12:10455309-10455310	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs187464281	chr12:10455327-10455328	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs149356901	chr12:10455351-10455352	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs386760266	chr12:10455366-10455367	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs76975516	chr12:10455368-10455369	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs201926634	chr12:10455371-10455372	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs76174037	chr12:10455372-10455373	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs550930948	chr12:10455382-10455383	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs144668311	chr12:10455400-10455401	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs74686241	chr12:10455487-10455488	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs553450070	chr12:10455489-10455490	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs566959603	chr12:10455495-10455496	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs367575999	chr12:10455565-10455566	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs535996415	chr12:10455572-10455573	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1995 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10447400-10455000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr12:10447800-10456600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr12:10453200-10461000	Weak transcription	Placenta	Placenta
4	chr12:10453400-10454600	Enhancers	Thymus	Thymus
5	chr12:10453400-10457000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr12:10453600-10454600	Enhancers	Primary T cells from cord blood	blood
7	chr12:10453800-10457200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:10454200-10458000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr12:10454400-10455600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr12:10454600-10455200	Weak transcription	Thymus	Thymus
11	chr12:10454800-10474400	Weak transcription	Left Ventricle	heart
12	chr12:10455000-10456000	Enhancers	Primary T cells fromperipheralblood	blood
13	chr12:10455200-10455400	ZNF genes & repeats	Thymus	Thymus
14	chr12:10455600-10455800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr12:10455800-10456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr12:10456000-10457000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr12:10456200-10456400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr12:10456200-10457200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:10456400-10457200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr12:10456400-10457800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr12:10456600-10457200	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr12:10457000-10457400	Enhancers	Primary T cells fromperipheralblood	blood
23	chr12:10457200-10457600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr12:10457200-10458000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr12:10457400-10458000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:10457400-10458000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr12:10457600-10458200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr12:10457600-10458200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr12:10457600-10458200	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr12:10457600-10458400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr12:10457800-10458400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10458000-10458400	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr12:10458000-10458400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:10458000-10464200	Active TSS	Primary T cells fromperipheralblood	blood
35	chr12:10458200-10460600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr12:10458400-10458800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
37	chr12:10458400-10460400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr12:10458800-10461200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:10460000-10460800	Active TSS	Primary B cells from cord blood	blood
40	chr12:10460200-10460600	Enhancers	Dnd41	blood
41	chr12:10460200-10460800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:10460400-10461600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:10460400-10463200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr12:10460600-10461400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:10460600-10462200	Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr12:10461000-10461200	Weak transcription	Primary B cells from cord blood	blood
47	chr12:10461000-10463200	Strong transcription	Placenta	Placenta
48	chr12:10461200-10467400	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
49	chr12:10461400-10461600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr12:10461600-10461800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood

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