Variant report

Variant	rs17585060
Chromosome Location	chr5:35357464-35357465
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10512631	0.85[EUR][1000 genomes]
rs16873191	0.85[EUR][1000 genomes]
rs16873210	0.85[EUR][1000 genomes]
rs16873529	0.92[EUR][1000 genomes]
rs16873766	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17438666	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17585046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs26196	1.00[EUR][1000 genomes]
rs56967971	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58975450	0.92[EUR][1000 genomes]
rs59862556	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61687847	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73087009	0.92[EUR][1000 genomes]
rs73087012	0.92[EUR][1000 genomes]
rs73087013	0.92[EUR][1000 genomes]
rs73087019	0.92[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35355200-35363600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:35355400-35358000	Weak transcription	H1 BMP4 Derived Trophoblast 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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