Variant report

Variant	rs55873439
Chromosome Location	chr6:55050595-55050596
allele	A/G
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]
rs10498801	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10948893	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10948894	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12526414	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12662510	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12663056	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2998995	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3006854	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3122148	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3122149	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs3122151	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3122152	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3134689	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3134690	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3134691	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3134692	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3134694	0.87[ASN][1000 genomes]
rs3134696	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3134699	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3134700	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3134701	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3134703	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4236127	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58828550	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59420753	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59682791	0.83[AMR][1000 genomes]
rs59867521	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60304167	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs60550710	0.95[ASN][1000 genomes]
rs62418310	0.95[ASN][1000 genomes]
rs62418311	0.94[ASN][1000 genomes]
rs6922310	0.81[AMR][1000 genomes]
rs6927478	0.90[ASN][1000 genomes]
rs6937705	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6937878	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6939376	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73434718	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73743300	0.87[EUR][1000 genomes]
rs7758861	0.92[ASN][1000 genomes]
rs7775741	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7775745	0.82[ASN][1000 genomes]
rs9367622	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9475199	0.89[EUR][1000 genomes]
rs9475200	0.89[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	nsv1016461	chr6:55038131-55129663	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island 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	chr6:55048200-55051000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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