Variant report

Variant	rs10493457
Chromosome Location	chr1:70335657-70335658
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11209521	1.00[CEU][hapmap]
rs12754604	0.82[YRI][hapmap]
rs17131058	0.80[YRI][hapmap];1.00[AMR][1000 genomes]
rs17131083	0.85[LWK][hapmap];0.80[YRI][hapmap]
rs17131089	0.85[LWK][hapmap];1.00[AMR][1000 genomes]
rs17131092	1.00[EUR][1000 genomes]
rs17131128	0.86[ASW][hapmap];1.00[AMR][1000 genomes]
rs17131130	1.00[CEU][hapmap]
rs2025896	0.83[YRI][hapmap]
rs35373978	1.00[EUR][1000 genomes]
rs74084506	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74084562	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74087763	1.00[EUR][1000 genomes]
rs7520980	0.80[YRI][hapmap];1.00[AMR][1000 genomes]
rs7546018	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7548343	1.00[CEU][hapmap];0.91[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][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	nsv428466	chr1:70306638-70455357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 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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