Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1430921	0.85[EUR][1000 genomes]
rs1594436	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1624685	0.81[EUR][1000 genomes]
rs1964354	0.86[EUR][1000 genomes]
rs28584921	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs628514	0.81[EUR][1000 genomes]
rs629764	0.81[EUR][1000 genomes]
rs639272	0.88[EUR][1000 genomes]
rs643272	0.86[EUR][1000 genomes]
rs647853	0.86[EUR][1000 genomes]
rs6507493	0.94[EUR][1000 genomes]
rs657288	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7230753	0.89[EUR][1000 genomes]
rs7239418	0.89[EUR][1000 genomes]
rs7239950	0.89[EUR][1000 genomes]
rs7244619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7245308	0.86[EUR][1000 genomes]
rs725744	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8089843	0.86[EUR][1000 genomes]
rs8094466	0.82[ASN][1000 genomes]
rs9304274	0.94[EUR][1000 genomes]
rs9807482	0.86[EUR][1000 genomes]
rs9944932	0.94[EUR][1000 genomes]
rs9951065	0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs9955757	0.93[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	esv3447158	chr18:40045478-40320720	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:40179600-40186600	Weak transcription	Adipose Nuclei	Adipose
2	chr18:40186400-40187600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:40186400-40187600	Enhancers	Fetal Muscle Leg	muscle

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