Variant report

Variant	rs1493755
Chromosome Location	chr12:44792000-44792001
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10506245	1.00[JPT][hapmap]
rs10880632	0.94[ASN][1000 genomes]
rs11182486	0.94[ASN][1000 genomes]
rs11182490	0.94[ASN][1000 genomes]
rs11182493	0.94[ASN][1000 genomes]
rs11182495	0.94[ASN][1000 genomes]
rs11182496	0.94[ASN][1000 genomes]
rs11182497	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182501	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182517	0.81[ASN][1000 genomes]
rs11611818	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11612521	0.94[ASN][1000 genomes]
rs12297907	0.94[ASN][1000 genomes]
rs12301564	0.94[ASN][1000 genomes]
rs12308701	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12308760	0.94[ASN][1000 genomes]
rs12308816	0.82[ASN][1000 genomes]
rs12310262	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12311228	0.94[ASN][1000 genomes]
rs12317228	0.94[ASN][1000 genomes]
rs12318553	0.94[ASN][1000 genomes]
rs12319211	0.94[ASN][1000 genomes]
rs12319354	0.94[ASN][1000 genomes]
rs1353143	0.88[ASN][1000 genomes]
rs1353145	0.94[ASN][1000 genomes]
rs1353146	0.94[ASN][1000 genomes]
rs1353147	0.94[ASN][1000 genomes]
rs1527315	1.00[JPT][hapmap]
rs1643432	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs17094634	0.94[ASN][1000 genomes]
rs17094695	0.81[ASN][1000 genomes]
rs17121322	0.94[ASN][1000 genomes]
rs1716605	1.00[JPT][hapmap]
rs1716609	1.00[JPT][hapmap]
rs1726879	0.87[EUR][1000 genomes]
rs1726884	1.00[JPT][hapmap]
rs1726888	0.82[EUR][1000 genomes]
rs1726889	1.00[JPT][hapmap]
rs1798023	1.00[JPT][hapmap]
rs1798032	1.00[JPT][hapmap]
rs1873978	0.94[ASN][1000 genomes]
rs1873980	0.94[ASN][1000 genomes]
rs1873981	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4639992	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4768559	1.00[JPT][hapmap]
rs55781129	0.81[ASN][1000 genomes]
rs55962853	0.81[ASN][1000 genomes]
rs56020032	0.81[ASN][1000 genomes]
rs56115011	0.94[ASN][1000 genomes]
rs56318423	0.81[ASN][1000 genomes]
rs59255697	0.81[ASN][1000 genomes]
rs60837979	0.81[ASN][1000 genomes]
rs68107418	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7132743	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7134756	0.94[ASN][1000 genomes]
rs7299010	0.81[ASN][1000 genomes]
rs7302676	0.81[ASN][1000 genomes]
rs73094334	0.94[ASN][1000 genomes]
rs7309948	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7314412	1.00[JPT][hapmap]
rs74085067	0.81[ASN][1000 genomes]
rs74085071	0.81[ASN][1000 genomes]
rs74085073	0.81[ASN][1000 genomes]
rs74085078	0.81[ASN][1000 genomes]
rs751921	0.94[ASN][1000 genomes]
rs7953681	0.81[ASN][1000 genomes]
rs7957832	0.81[ASN][1000 genomes]
rs7958300	0.81[ASN][1000 genomes]
rs7958770	0.81[ASN][1000 genomes]
rs7960681	0.81[ASN][1000 genomes]
rs7961768	0.85[EUR][1000 genomes]
rs7962332	0.94[ASN][1000 genomes]
rs7964751	0.94[ASN][1000 genomes]
rs7965110	0.94[ASN][1000 genomes]
rs7965383	0.94[ASN][1000 genomes]
rs7969400	0.94[ASN][1000 genomes]
rs7969428	0.94[ASN][1000 genomes]
rs7969466	1.00[JPT][hapmap]
rs7969614	1.00[ASN][1000 genomes]
rs7970601	0.81[ASN][1000 genomes]
rs7971520	0.81[ASN][1000 genomes]
rs7972882	0.94[ASN][1000 genomes]
rs7978776	0.94[ASN][1000 genomes]
rs7979642	0.81[ASN][1000 genomes]
rs840764	0.83[EUR][1000 genomes]
rs840772	0.93[CEU][hapmap];0.99[EUR][1000 genomes]
rs840773	1.00[JPT][hapmap]
rs840774	1.00[JPT][hapmap]
rs859016	1.00[JPT][hapmap]
rs863482	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1038498	chr12:44679455-44816572	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44791000-44792200	Enhancers	Brain Germinal Matrix	brain
2	chr12:44791600-44792200	Enhancers	Right Atrium	heart
3	chr12:44791800-44792600	Enhancers	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links