Variant report

Variant	rs12046244
Chromosome Location	chr1:220662588-220662589
allele	C/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]
rs10495147	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11118567	0.82[ASW][hapmap]
rs11118573	0.82[ASW][hapmap]
rs2152836	0.82[ASW][hapmap]
rs2889895	0.88[ASW][hapmap]
rs3753873	0.83[JPT][hapmap]
rs3753874	0.86[ASW][hapmap];0.83[JPT][hapmap]
rs3767323	0.82[ASW][hapmap]
rs3842967	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4120669	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4846326	0.82[ASW][hapmap]
rs4846647	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7548893	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7555225	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220658600-220665800	Weak transcription	Adipose Nuclei	Adipose

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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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