Variant report

Variant	rs74139837
Chromosome Location	chr1:227024891-227024892
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16846590	0.80[AFR][1000 genomes]
rs58698650	0.80[AFR][1000 genomes]
rs59683545	0.80[AFR][1000 genomes]
rs60602411	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61103575	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61185121	0.80[AFR][1000 genomes]
rs61674281	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74139805	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74139806	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74139812	1.00[AMR][1000 genomes]
rs74139838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74139840	1.00[AMR][1000 genomes]
rs74139842	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227024600-227026000	Enhancers	Hela-S3	cervix

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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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