Variant report

Variant	rs12338395
Chromosome Location	chr9:84498407-84498408
allele	C/T
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]
rs12336197	0.86[AMR][1000 genomes]
rs12345231	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12345266	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12351812	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1334759	0.95[AMR][1000 genomes]
rs1413797	0.87[AMR][1000 genomes]
rs1855607	0.95[AMR][1000 genomes]
rs56281129	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56306550	0.86[AMR][1000 genomes]
rs57386263	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57921200	0.86[AMR][1000 genomes]
rs58931877	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60427225	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9886839	0.81[AMR][1000 genomes]
rs9987870	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:84495200-84499000	Weak transcription	Fetal Stomach	stomach
2	chr9:84495200-84500600	Weak transcription	Fetal Muscle Leg	muscle
3	chr9:84495600-84501200	Weak transcription	Fetal Lung	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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