Variant report

Variant	rs10787567
Chromosome Location	chr10:117106798-117106799
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11197173	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11498596	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12253499	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1264798	0.80[ASN][1000 genomes]
rs1494174	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1565833	0.92[ASN][1000 genomes]
rs2165988	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2201363	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2485966	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2485968	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2485971	0.92[ASN][1000 genomes]
rs2587461	0.80[EUR][1000 genomes]
rs594160	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs615905	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs675816	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs683117	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs703352	0.87[ASN][1000 genomes]
rs9630104	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9630105	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117099800-117109200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:117105000-117113400	Weak transcription	Aorta	Aorta

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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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