Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10035549	0.95[ASN][1000 genomes]
rs10050855	0.89[ASN][1000 genomes]
rs10478141	0.82[AMR][1000 genomes]
rs11241223	0.91[ASN][1000 genomes]
rs11241224	0.95[ASN][1000 genomes]
rs11241226	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12332749	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12332751	0.93[ASN][1000 genomes]
rs12521147	0.82[AMR][1000 genomes]
rs1384267	0.95[ASN][1000 genomes]
rs1384268	0.94[ASN][1000 genomes]
rs1384269	0.95[ASN][1000 genomes]
rs1384270	0.91[ASN][1000 genomes]
rs1482347	0.83[AMR][1000 genomes]
rs1552158	0.80[AMR][1000 genomes]
rs1842760	0.82[AMR][1000 genomes]
rs1871908	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1871909	0.95[ASN][1000 genomes]
rs1871912	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1988077	0.83[AMR][1000 genomes]
rs4235748	0.93[ASN][1000 genomes]
rs4285208	0.92[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4331886	0.95[ASN][1000 genomes]
rs4705469	0.82[AMR][1000 genomes]
rs4705470	0.80[AMR][1000 genomes]
rs6872692	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6891470	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7443933	0.93[ASN][1000 genomes]
rs985411	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[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	esv2081988	chr5:113054622-113054623	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113049200-113057400	Weak transcription	Fetal Kidney	kidney
2	chr5:113051000-113058200	Weak transcription	Fetal Lung	lung
3	chr5:113054000-113055000	Enhancers	Stomach Smooth Muscle	stomach
4	chr5:113054200-113055600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:113054400-113055400	Enhancers	Fetal Stomach	stomach
6	chr5:113054600-113058400	Weak transcription	Duodenum Smooth Muscle	Duodenum

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