Variant report

Variant	rs2950425
Chromosome Location	chr12:121812153-121812154
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1169963	0.82[EUR][1000 genomes]
rs1169964	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1617736	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2668261	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2668262	0.82[EUR][1000 genomes]
rs2911705	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2942069	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2942076	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2950426	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6489806	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7398507	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121810400-121814200	Weak transcription	HepG2	liver
2	chr12:121811400-121812200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	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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