Variant report

Variant	rs73017286
Chromosome Location	chr2:172048632-172048633
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs16859177	0.86[EUR][1000 genomes]
rs16859206	0.82[EUR][1000 genomes]
rs55991728	0.96[EUR][1000 genomes]
rs56134465	0.84[EUR][1000 genomes]
rs56216250	0.80[EUR][1000 genomes]
rs56243805	0.96[EUR][1000 genomes]
rs56267332	0.98[EUR][1000 genomes]
rs60730419	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61105084	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6711423	0.86[EUR][1000 genomes]
rs73013465	0.86[EUR][1000 genomes]
rs73017249	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73017262	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73017268	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73976125	0.86[EUR][1000 genomes]
rs7580756	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9752051	0.84[AMR][1000 genomes];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	chr2:172048200-172048800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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