Variant report

Variant	rs72795057
Chromosome Location	chr10:45036463-45036464
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11591669	0.86[ASN][1000 genomes]
rs11592569	0.89[ASN][1000 genomes]
rs11593437	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11593439	0.86[ASN][1000 genomes]
rs11593585	0.93[ASN][1000 genomes]
rs11593591	0.86[ASN][1000 genomes]
rs11595335	0.90[ASN][1000 genomes]
rs11595472	0.86[ASN][1000 genomes]
rs11596551	0.88[ASN][1000 genomes]
rs11597734	0.95[ASN][1000 genomes]
rs11598774	0.86[ASN][1000 genomes]
rs11598916	0.95[ASN][1000 genomes]
rs1572202	0.89[ASN][1000 genomes]
rs17156636	0.94[ASN][1000 genomes]
rs17407080	0.86[ASN][1000 genomes]
rs17407137	0.86[ASN][1000 genomes]
rs17407291	0.96[ASN][1000 genomes]
rs17408225	0.94[ASN][1000 genomes]
rs17485517	0.86[ASN][1000 genomes]
rs17485977	0.95[ASN][1000 genomes]
rs17486117	0.95[ASN][1000 genomes]
rs17487074	0.93[ASN][1000 genomes]
rs1977896	0.88[ASN][1000 genomes]
rs1977897	0.88[ASN][1000 genomes]
rs2184771	0.86[ASN][1000 genomes]
rs28373082	0.86[ASN][1000 genomes]
rs34071927	0.94[ASN][1000 genomes]
rs57991475	0.93[ASN][1000 genomes]
rs6593427	0.85[ASN][1000 genomes]
rs7084757	0.86[ASN][1000 genomes]
rs72795018	0.89[ASN][1000 genomes]
rs72795026	0.86[ASN][1000 genomes]
rs72795029	0.86[ASN][1000 genomes]
rs72795030	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72795035	0.86[ASN][1000 genomes]
rs72795036	0.86[ASN][1000 genomes]
rs72795038	0.86[ASN][1000 genomes]
rs72795039	0.86[ASN][1000 genomes]
rs72795043	0.88[ASN][1000 genomes]
rs72795059	1.00[ASN][1000 genomes]
rs72795073	0.96[ASN][1000 genomes]
rs72795078	0.95[ASN][1000 genomes]
rs72795079	0.92[ASN][1000 genomes]
rs7898623	0.83[ASN][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	esv3362044	chr10:45030252-45038251	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45035600-45037800	Weak transcription	Fetal Brain Male	brain

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