Variant report

Variant	rs9808471
Chromosome Location	chr2:74105293-74105294
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10519327	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11126420	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11885317	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11886615	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17009428	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs33990056	0.93[ASN][1000 genomes]
rs3738846	0.91[ASN][1000 genomes]
rs56383013	0.83[ASN][1000 genomes]
rs56801363	0.84[ASN][1000 genomes]
rs57394861	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61091264	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6726010	0.91[ASN][1000 genomes]
rs6737597	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7606408	0.84[ASN][1000 genomes]
rs9309477	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9808106	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74097600-74114600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:74104000-74105400	Enhancers	Primary monocytes fromperipheralblood	blood

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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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