Variant report

Variant	rs13032617
Chromosome Location	chr2:141312831-141312832
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1352046	0.84[MEX][hapmap]
rs1518440	0.91[MEX][hapmap]
rs1518444	0.84[MEX][hapmap]
rs17387292	0.91[MEX][hapmap]
rs17387536	0.91[MEX][hapmap]
rs1878741	0.84[MEX][hapmap]
rs41323147	0.84[MEX][hapmap]
rs41478345	0.84[MEX][hapmap]
rs6715219	0.91[MEX][hapmap]
rs7422845	0.91[MEX][hapmap]
rs7575460	0.91[MEX][hapmap]

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	nsv583192	chr2:141310721-141350100	Enhancers Weak transcription	Chromatin interactive region miRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141312600-141314000	Enhancers	Liver	Liver

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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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