Variant report

Variant	rs2593714
Chromosome Location	chr2:144626889-144626890
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17834684	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs787155	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs787156	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs787157	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs787158	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs787162	1.00[CEU][hapmap];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	chr2:144626200-144629200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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