Variant report

Variant	rs2950426
Chromosome Location	chr12:121812286-121812287
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1169964	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12303740	0.80[ASN][1000 genomes]
rs1617736	0.89[ASN][1000 genomes]
rs2668261	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2911705	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2942069	0.98[ASN][1000 genomes]
rs2942076	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2950425	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6489806	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7398507	0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121810400-121814200	Weak transcription	HepG2	liver
2	chr12:121812000-121815000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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