Variant report

Variant	rs74161622
Chromosome Location	chr10:117404322-117404323
allele	A/G
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]
rs10160074	1.00[EUR][1000 genomes]
rs11814126	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11814635	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11817708	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34243141	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55893753	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56844032	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60303530	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60532735	1.00[AMR][1000 genomes]
rs74158208	0.98[AFR][1000 genomes]
rs74158209	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74158390	1.00[AMR][1000 genomes]
rs74158392	1.00[AMR][1000 genomes]
rs74158398	1.00[AMR][1000 genomes]
rs74161603	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117404000-117404600	Enhancers	hESC Derived CD56+ Mesoderm 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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