Variant report

Variant	rs6982653
Chromosome Location	chr8:64758222-64758223
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12543529	0.86[ASN][1000 genomes]
rs12675807	0.92[ASN][1000 genomes]
rs13254613	0.91[ASN][1000 genomes]
rs1985894	0.86[ASN][1000 genomes]
rs4737661	0.86[ASN][1000 genomes]
rs6988399	0.86[ASN][1000 genomes]
rs6994250	0.92[ASN][1000 genomes]
rs705988	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs705990	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64757800-64762400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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