Variant report

Variant	rs10992728
Chromosome Location	chr9:96178668-96178669
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10992723	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2184255	0.89[EUR][1000 genomes]
rs2841680	0.91[ASN][1000 genomes]
rs2841681	0.90[ASN][1000 genomes]
rs4563950	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7020852	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72743489	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96176600-96179200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:96178200-96181000	Enhancers	Placenta	Placenta
3	chr9:96178600-96179000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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