Variant report

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

rs_ID	r²[population]
rs13241576	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs13241764	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs17133160	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2237640	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237641	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2237642	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2237644	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2283030	0.80[AMR][1000 genomes]
rs2283031	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2283032	0.80[AMR][1000 genomes]
rs2283033	0.80[AMR][1000 genomes]
rs2283034	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs35093250	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs62482298	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62482299	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62482324	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62482325	0.95[EUR][1000 genomes]
rs62482327	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6944413	0.98[EUR][1000 genomes]
rs6949057	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7784567	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7784979	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7784991	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7803462	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7807415	0.93[AFR][1000 genomes];0.80[AMR][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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103520800-103529200	Weak transcription	HepG2	liver
2	chr7:103524200-103526800	Weak transcription	K562	blood

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