Variant report

Variant	rs3808124
Chromosome Location	chr7:126690946-126690947
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11563357	0.82[JPT][hapmap]
rs12375090	0.82[JPT][hapmap]
rs17862330	1.00[CEU][hapmap]
rs17863225	1.00[CEU][hapmap]
rs17867779	1.00[CEU][hapmap]
rs3808125	1.00[CEU][hapmap]
rs6977479	0.82[JPT][hapmap]
rs7782188	1.00[YRI][hapmap]
rs7808572	1.00[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	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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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