Variant report

Variant	rs62429273
Chromosome Location	chr6:133975570-133975571
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11961183	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12207040	0.85[ASN][1000 genomes]
rs12209147	0.85[ASN][1000 genomes]
rs12661401	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13218156	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55786252	0.82[EUR][1000 genomes]
rs62427513	0.82[EUR][1000 genomes]
rs62427514	0.82[EUR][1000 genomes]
rs62427515	0.82[EUR][1000 genomes]
rs62427516	0.82[EUR][1000 genomes]
rs6907934	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6914525	0.84[EUR][1000 genomes]
rs6933141	0.97[ASN][1000 genomes]
rs7765837	0.83[EUR][1000 genomes]
rs9493674	0.82[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133970400-133976000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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