Variant report

Variant	rs9799426
Chromosome Location	chr2:219040117-219040118
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10023738	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28369225	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs34456247	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35734535	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs56412716	0.91[ASN][1000 genomes]
rs7694391	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9799794	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:219034800-219041200	Weak transcription	Stomach Mucosa	stomach
2	chr2:219038000-219044600	Weak transcription	Placenta	Placenta

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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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