Variant report

Variant	rs7711606
Chromosome Location	chr5:29850525-29850526
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12697227	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1428318	0.93[AMR][1000 genomes]
rs1428321	0.93[AMR][1000 genomes]
rs16899550	0.93[AMR][1000 genomes]
rs72745276	0.93[AMR][1000 genomes]
rs72745277	0.93[AMR][1000 genomes]
rs72745278	0.91[AMR][1000 genomes]
rs72745295	0.93[AMR][1000 genomes]
rs7449322	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9292344	0.93[AMR][1000 genomes]
rs9790891	0.93[AMR][1000 genomes]
rs9791032	0.93[AMR][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	esv3385368	chr5:29548608-29910057	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	10 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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