Variant report

Variant	rs6706672
Chromosome Location	chr2:37399351-37399352
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]
rs13022403	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2540974	0.82[EUR][1000 genomes]
rs3845786	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4670670	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4670671	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4670674	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6710046	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6734866	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6748151	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37398800-37399400	Enhancers	HepG2	liver

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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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