Variant report

Variant	rs13361967
Chromosome Location	chr5:91790066-91790067
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12515713	0.89[ASN][1000 genomes]
rs13168674	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28599560	0.84[ASN][1000 genomes]
rs34135545	0.88[ASN][1000 genomes]
rs34957590	0.88[ASN][1000 genomes]
rs35148225	0.89[ASN][1000 genomes]
rs35280400	0.82[EUR][1000 genomes]
rs36081011	0.88[ASN][1000 genomes]
rs36097806	0.88[ASN][1000 genomes]
rs4260649	0.88[ASN][1000 genomes]
rs4351128	0.88[ASN][1000 genomes]
rs4869411	0.88[ASN][1000 genomes]
rs55908760	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60306725	0.84[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	esv2763469	chr5:91759081-91812497	Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91790000-91790400	Enhancers	GM12878-XiMat	blood

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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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