Variant report

Variant	rs7585692
Chromosome Location	chr2:124841838-124841839
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10496623	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10496625	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs12614779	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs12622072	0.87[CEU][hapmap];0.80[CHB][hapmap];1.00[YRI][hapmap]
rs13425875	0.81[EUR][1000 genomes]
rs17010743	0.81[AMR][1000 genomes]
rs17010744	0.87[CEU][hapmap];0.81[AMR][1000 genomes]
rs17010780	0.87[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs17010809	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17010810	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17010817	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[YRI][hapmap]
rs17010819	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17010881	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs4848235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4848911	0.87[CEU][hapmap];1.00[YRI][hapmap]
rs55718116	1.00[AFR][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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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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