Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1001882	0.88[EUR][1000 genomes]
rs17529213	0.83[EUR][1000 genomes]
rs2050447	0.91[EUR][1000 genomes]
rs2281	0.90[EUR][1000 genomes]
rs2992257	0.88[EUR][1000 genomes]
rs2992258	0.89[EUR][1000 genomes]
rs2992264	0.87[EUR][1000 genomes]
rs2992265	0.87[EUR][1000 genomes]
rs2992267	0.87[EUR][1000 genomes]
rs2992297	0.87[EUR][1000 genomes]
rs2992298	0.88[EUR][1000 genomes]
rs2992326	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2992327	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3006785	0.88[EUR][1000 genomes]
rs3006803	0.89[EUR][1000 genomes]
rs3006804	0.91[EUR][1000 genomes]
rs3006805	0.90[EUR][1000 genomes]
rs3006809	0.87[EUR][1000 genomes]
rs3006812	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3006814	0.92[EUR][1000 genomes]
rs3006817	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3006820	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3006822	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3006824	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3006833	0.87[EUR][1000 genomes]
rs703007	0.87[EUR][1000 genomes]
rs7901931	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs871367	0.88[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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv1043832	chr10:26669040-26809400	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:26711400-26713400	Enhancers	Primary monocytes fromperipheralblood	blood

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