Variant report

Variant	rs72876910
Chromosome Location	chr11:26328044-26328045
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17308992	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2100820	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55642080	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56131609	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56347193	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72874951	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72874968	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72874981	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72874983	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72874987	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72876907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72876916	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3425701	chr11:26310425-26330495	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26328000-26328400	Enhancers	Foreskin Fibroblast 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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