Variant report

Variant	rs6780244
Chromosome Location	chr3:178620627-178620628
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]
rs10936980	0.81[JPT][hapmap]
rs10936982	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10936984	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11712366	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11713575	0.96[ASN][1000 genomes]
rs13095781	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4621308	0.81[JPT][hapmap]
rs6443590	0.81[JPT][hapmap]
rs6443601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6770789	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6773785	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6782524	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7428095	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7624064	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178618800-178628000	Weak transcription	Brain Hippocampus Middle	brain

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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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