Variant report

Variant	rs1601060
Chromosome Location	chr8:63066028-63066029
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10094813	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10096468	0.83[ASN][1000 genomes]
rs10108722	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10110503	0.94[ASN][1000 genomes]
rs1384680	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1483181	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1483182	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1825308	0.81[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2351436	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2351643	0.88[ASN][1000 genomes]
rs2351644	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4738940	0.87[ASN][1000 genomes]
rs6471997	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs900493	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63061200-63072200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:63064400-63066600	Weak transcription	Hela-S3	cervix

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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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