Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10754022	0.96[EUR][1000 genomes]
rs10754023	0.96[EUR][1000 genomes]
rs10801140	0.89[EUR][1000 genomes]
rs10921233	0.94[EUR][1000 genomes]
rs10921234	0.89[EUR][1000 genomes]
rs10921236	0.81[EUR][1000 genomes]
rs10921237	0.93[EUR][1000 genomes]
rs10921238	0.88[EUR][1000 genomes]
rs10921239	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11576197	0.91[EUR][1000 genomes]
rs12037932	0.87[EUR][1000 genomes]
rs12042114	0.95[EUR][1000 genomes]
rs12118386	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12403636	0.95[EUR][1000 genomes]
rs1933705	0.88[EUR][1000 genomes]
rs1933706	0.88[EUR][1000 genomes]
rs1933709	0.89[ASN][1000 genomes]
rs1933711	0.90[ASN][1000 genomes]
rs1933712	0.96[EUR][1000 genomes]
rs1933713	0.96[EUR][1000 genomes]
rs1933714	0.95[EUR][1000 genomes]
rs1933715	0.96[EUR][1000 genomes]
rs2104248	0.84[EUR][1000 genomes]
rs2146607	0.88[EUR][1000 genomes]
rs2181445	0.89[EUR][1000 genomes]
rs2208960	0.96[EUR][1000 genomes]
rs2369892	0.91[EUR][1000 genomes]
rs6695451	0.87[EUR][1000 genomes]
rs6702192	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7540755	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7549322	0.96[EUR][1000 genomes]
rs961480	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532618	chr1:192537006-193149179	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv548660	chr1:192609268-192945348	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 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	chr1:192638200-192644000	Weak transcription	Pancreas	Pancrea

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