Variant report

Variant	rs10504344
Chromosome Location	chr8:63066784-63066785
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12544805	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1601056	0.85[EUR][1000 genomes]
rs34250977	0.93[EUR][1000 genomes]
rs4256587	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4268118	0.91[EUR][1000 genomes]
rs4317559	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4383956	0.92[EUR][1000 genomes]
rs4445217	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4562310	0.91[EUR][1000 genomes]
rs4610738	0.91[EUR][1000 genomes]
rs4738938	0.91[EUR][1000 genomes]
rs4738939	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6980515	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7462666	0.83[EUR][1000 genomes]
rs7832144	0.93[EUR][1000 genomes]
rs7841863	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:3 , 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	chr8:63066600-63067000	Enhancers	A549	lung
3	chr8:63066600-63067800	Enhancers	Hela-S3	cervix

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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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