Variant report

Variant	rs4926708
Chromosome Location	chr1:56515872-56515873
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10158150	0.84[EUR][1000 genomes]
rs11206731	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11206735	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12025982	0.83[EUR][1000 genomes]
rs12041298	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12131359	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1331855	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1331856	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1412215	0.86[EUR][1000 genomes]
rs1998715	0.87[ASN][1000 genomes]
rs2404393	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4926707	0.81[EUR][1000 genomes]
rs56845669	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6670027	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6675451	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7525207	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7551693	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9436997	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56499600-56522200	Weak transcription	Placenta	Placenta
2	chr1:56510000-56516400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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