Variant report

Variant	rs1582186
Chromosome Location	chr6:109530939-109530940
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs13207770	0.97[ASN][1000 genomes]
rs1582187	0.97[ASN][1000 genomes]
rs59580934	0.80[AFR][1000 genomes]
rs6928327	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73762659	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73762660	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73762661	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73762693	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7742743	0.97[ASN][1000 genomes]
rs7754785	0.97[ASN][1000 genomes]
rs7755242	0.97[ASN][1000 genomes]
rs9487007	0.97[ASN][1000 genomes]
rs9487008	0.97[ASN][1000 genomes]
rs9487009	0.97[ASN][1000 genomes]
rs9487012	0.87[AFR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109516400-109535000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:109517200-109544800	Weak transcription	Psoas Muscle	Psoas

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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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