Variant report

Variant	rs4256080
Chromosome Location	chr3:60697526-60697527
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1716720	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1716744	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1716745	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1735460	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1735461	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1735462	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1735464	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1735469	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1735470	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1735471	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9819311	0.85[YRI][hapmap]
rs9865526	0.84[YRI][hapmap]
rs9866066	0.84[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links