Variant report

Variant	rs1072699
Chromosome Location	chr7:104311265-104311266
allele	A/G
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]
rs10953443	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs11761950	1.00[CHB][hapmap]
rs11768912	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12705266	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs6951477	0.87[CEU][hapmap]
rs6974634	0.91[EUR][1000 genomes]
rs73181859	0.90[EUR][1000 genomes]
rs7812002	0.93[CEU][hapmap];0.91[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	nsv970927	chr7:104307903-104312412	Inactive region	TF binding region CpG island Chromatin interactive region	1 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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