Variant report

Variant	rs59943811
Chromosome Location	chr8:129977730-129977731
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs16893221	0.83[ASN][1000 genomes]
rs16903928	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57247106	0.86[ASN][1000 genomes]
rs60730791	0.86[ASN][1000 genomes]
rs6995520	0.83[ASN][1000 genomes]
rs73708261	1.00[ASN][1000 genomes]
rs7821793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs882082	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs882084	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs894264	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129970800-129982400	Weak transcription	HSMM	muscle
2	chr8:129977000-129978800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:129977000-129981400	Weak transcription	Dnd41	blood
4	chr8:129977000-129985000	Weak transcription	Psoas Muscle	Psoas
5	chr8:129977200-129978400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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