Variant report

Variant	rs12219425
Chromosome Location	chr10:44333491-44333492
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10793501	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10899918	0.87[EUR][1000 genomes]
rs1870636	0.86[AFR][1000 genomes]
rs2085798	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4948781	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4948783	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs729247	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs748715	0.83[AFR][1000 genomes]
rs912804	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44332000-44337200	Weak transcription	Pancreas	Pancrea

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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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