Variant report

Variant	rs6465990
Chromosome Location	chr7:104112261-104112262
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10216261	0.84[YRI][hapmap]
rs1034572	0.96[CEU][hapmap]
rs17137948	0.96[CEU][hapmap];0.83[CHB][hapmap]
rs6949376	0.92[CEU][hapmap];0.81[YRI][hapmap];0.86[EUR][1000 genomes]
rs6949536	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs6949602	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs6949811	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6955069	0.86[CEU][hapmap]
rs6965697	0.96[CEU][hapmap];0.96[YRI][hapmap]
rs7776632	0.80[YRI][hapmap]

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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