Variant report

Variant	rs57140603
Chromosome Location	chr10:26472308-26472309
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10508713	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11812370	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11815755	1.00[EUR][1000 genomes]
rs11816461	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11816664	0.82[AMR][1000 genomes]
rs11817896	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16926590	0.82[AMR][1000 genomes]
rs16926628	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16926660	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16926667	1.00[EUR][1000 genomes]
rs17666893	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17667157	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17739436	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17739453	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17739680	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1935485	1.00[ASN][1000 genomes]
rs2222351	0.82[AMR][1000 genomes]
rs3897758	0.85[AMR][1000 genomes]
rs41279908	0.85[AMR][1000 genomes]
rs4370835	0.85[AMR][1000 genomes]
rs56153367	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56234810	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs57687518	0.82[AMR][1000 genomes]
rs58309865	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58990448	1.00[EUR][1000 genomes]
rs59646929	0.85[AMR][1000 genomes]
rs61284099	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6650135	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7074143	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7082557	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72787349	0.85[AMR][1000 genomes]
rs72787350	0.85[AMR][1000 genomes]
rs72789947	0.82[AMR][1000 genomes]
rs72789954	0.85[AMR][1000 genomes]
rs72789957	0.82[AMR][1000 genomes]
rs72789960	0.82[AMR][1000 genomes]
rs72793209	0.85[AMR][1000 genomes]
rs72793210	0.85[AMR][1000 genomes]
rs72793214	0.85[AMR][1000 genomes]
rs72793215	0.82[AMR][1000 genomes]
rs72793218	0.82[AMR][1000 genomes]
rs72793940	0.85[AMR][1000 genomes]
rs72793945	0.82[AMR][1000 genomes]
rs72793992	0.85[AMR][1000 genomes]
rs74126361	0.85[AMR][1000 genomes]
rs74126386	0.82[AMR][1000 genomes]
rs74126397	0.85[AMR][1000 genomes]
rs74126400	0.82[AMR][1000 genomes]
rs74126401	0.82[AMR][1000 genomes]
rs74126402	0.85[AMR][1000 genomes]
rs74129103	0.82[AMR][1000 genomes]
rs74129107	0.81[EUR][1000 genomes]
rs74129109	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs74129112	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs74129113	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7894269	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7909349	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7919609	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26440800-26473400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26464600-26478000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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