Variant report

Variant	rs3120156
Chromosome Location	chr1:71188712-71188713
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1327452	0.90[EUR][1000 genomes]
rs1327462	0.93[EUR][1000 genomes]
rs1409979	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1409980	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1409986	0.84[EUR][1000 genomes]
rs1414069	0.88[EUR][1000 genomes]
rs1591385	0.97[EUR][1000 genomes]
rs1854149	0.96[EUR][1000 genomes]
rs2209747	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2225110	0.96[EUR][1000 genomes]
rs2257713	0.96[EUR][1000 genomes]
rs2258725	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2782785	1.00[EUR][1000 genomes]
rs3131374	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs3131375	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6424406	0.88[EUR][1000 genomes]
rs7515193	0.93[EUR][1000 genomes]
rs7525012	0.94[EUR][1000 genomes]
rs7551638	0.94[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71184000-71193000	Weak transcription	Aorta	Aorta

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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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