Variant report

Variant	rs59167655
Chromosome Location	chr2:125348696-125348697
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1454139	0.82[EUR][1000 genomes]
rs1504016	0.94[EUR][1000 genomes]
rs17011851	0.82[EUR][1000 genomes]
rs17011859	0.82[EUR][1000 genomes]
rs17011865	0.82[EUR][1000 genomes]
rs66820110	0.82[EUR][1000 genomes]
rs72841382	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72841384	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72841386	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72841388	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72841390	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72845015	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72845026	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72845059	0.82[EUR][1000 genomes]
rs72845077	0.82[EUR][1000 genomes]
rs72845078	0.82[EUR][1000 genomes]
rs72845079	0.82[EUR][1000 genomes]
rs72845081	0.82[EUR][1000 genomes]
rs72845252	0.82[EUR][1000 genomes]
rs72845253	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72845255	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72845257	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72845874	0.82[EUR][1000 genomes]
rs72845877	0.82[EUR][1000 genomes]
rs72845878	0.82[EUR][1000 genomes]
rs72845884	0.82[EUR][1000 genomes]

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	nsv1014610	chr2:125124983-125350342	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv834357	chr2:125258157-125421507	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv528674	chr2:125346337-125383522	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125348000-125349000	Enhancers	Fetal Intestine Large	intestine
2	chr2:125348200-125349200	Weak transcription	Fetal Intestine Small	intestine

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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

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