Variant report

Variant	rs17137758
Chromosome Location	chr7:104099931-104099932
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17137736	0.93[YRI][hapmap]
rs4730008	1.00[JPT][hapmap]
rs57941093	0.97[ASN][1000 genomes]
rs58508368	1.00[ASN][1000 genomes]
rs58876754	0.97[ASN][1000 genomes]
rs59883984	0.97[ASN][1000 genomes]
rs60680884	0.97[ASN][1000 genomes]
rs6960997	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	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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