Variant report

Variant	rs35055513
Chromosome Location	chr8:129834676-129834677
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12541496	0.95[AMR][1000 genomes]
rs12541508	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12544345	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12548853	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12549424	0.90[AMR][1000 genomes]
rs12549751	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13250924	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13257555	0.82[AMR][1000 genomes]
rs13269648	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13273255	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13275784	0.90[AMR][1000 genomes]
rs13280887	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2028517	0.86[AMR][1000 genomes]
rs34093858	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34757177	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34825160	0.86[AMR][1000 genomes]
rs35081453	0.86[AMR][1000 genomes]
rs35181074	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35296092	0.86[AMR][1000 genomes]
rs35299722	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35697214	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35950030	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs36040241	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36141457	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs36142507	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56884764	0.86[AMR][1000 genomes]
rs57630172	0.90[AMR][1000 genomes]
rs61025881	0.82[AMR][1000 genomes]
rs61580176	0.82[AMR][1000 genomes]
rs67628488	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73373832	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73385409	1.00[AMR][1000 genomes];0.82[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	esv2578193	chr8:129833526-129834947	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129825400-129836800	Weak transcription	Dnd41	blood

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