Variant report

Variant	rs10132214
Chromosome Location	chr14:63464096-63464097
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1007062	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs10129513	0.88[CEU][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap]
rs10130015	0.94[CEU][hapmap];0.86[EUR][1000 genomes]
rs10131734	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10132410	0.94[CEU][hapmap]
rs10133358	0.88[CEU][hapmap]
rs10139542	0.87[CEU][hapmap]
rs10141458	0.94[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs10142476	0.94[CEU][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10142809	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11158468	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs11158469	0.82[CEU][hapmap]
rs11624884	0.87[CEU][hapmap]
rs12147350	0.90[EUR][1000 genomes]
rs12587142	0.88[CHB][hapmap]
rs12587171	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs12589987	0.93[EUR][1000 genomes]
rs1950986	0.94[CEU][hapmap]
rs1950987	0.82[CEU][hapmap]
rs1950988	0.88[CEU][hapmap];0.88[CHB][hapmap];0.81[ASN][1000 genomes]
rs1950989	0.88[CEU][hapmap]
rs1950990	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs1956673	0.82[CEU][hapmap]
rs1956679	0.93[EUR][1000 genomes]
rs28376422	0.92[ASN][1000 genomes]
rs28490569	0.90[EUR][1000 genomes]
rs3906692	0.82[CEU][hapmap]
rs3906693	0.87[CEU][hapmap]
rs3910327	0.82[CEU][hapmap]
rs3910328	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs3910329	0.88[CEU][hapmap];0.89[CHB][hapmap];0.86[ASN][1000 genomes]
rs4257136	0.86[ASN][1000 genomes]
rs4635259	0.86[ASN][1000 genomes]
rs5010674	0.88[CEU][hapmap]
rs5010675	0.86[CEU][hapmap]
rs5010676	0.87[CEU][hapmap]
rs6573468	0.82[CEU][hapmap]
rs6573475	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs6573476	0.82[CEU][hapmap]
rs6573477	0.81[CHB][hapmap]
rs67610164	0.92[EUR][1000 genomes]
rs7140971	0.90[EUR][1000 genomes]
rs7141489	0.93[ASN][1000 genomes]
rs7154634	0.82[CEU][hapmap]
rs7157827	0.86[ASN][1000 genomes]
rs7159483	0.88[CEU][hapmap]
rs7159948	0.88[CEU][hapmap]
rs7160761	0.88[CEU][hapmap]
rs717059	0.82[CEU][hapmap]
rs72728802	0.90[ASN][1000 genomes]
rs72730205	0.89[ASN][1000 genomes]
rs8004263	0.82[CHB][hapmap]
rs8004870	0.94[CEU][hapmap];0.92[EUR][1000 genomes]
rs8005258	0.83[CHB][hapmap]
rs8006836	0.93[EUR][1000 genomes]
rs8018212	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs8021399	0.84[CHB][hapmap]
rs9323430	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs9652353	0.89[ASN][1000 genomes]
rs9652354	0.89[ASN][1000 genomes]

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	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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