Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10195210	0.83[ASN][1000 genomes]
rs10497936	0.95[ASN][1000 genomes]
rs12611962	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12619699	0.83[ASN][1000 genomes]
rs12620783	0.95[ASN][1000 genomes]
rs12620896	0.87[ASN][1000 genomes]
rs12694230	0.82[ASN][1000 genomes]
rs13025294	0.81[ASN][1000 genomes]
rs13389611	0.82[ASN][1000 genomes]
rs13419011	0.83[ASN][1000 genomes]
rs13432611	0.83[ASN][1000 genomes]
rs13432618	0.83[ASN][1000 genomes]
rs1437916	0.89[ASN][1000 genomes]
rs1465827	0.95[ASN][1000 genomes]
rs1465828	0.93[ASN][1000 genomes]
rs16845716	0.97[ASN][1000 genomes]
rs1836732	0.82[ASN][1000 genomes]
rs2043790	0.98[ASN][1000 genomes]
rs4673601	0.95[ASN][1000 genomes]
rs57474880	0.89[ASN][1000 genomes]
rs71422736	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460064	chr2:212045919-212101698	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv470511	chr2:212045919-212101698	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv584312	chr2:212045919-212101698	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv834522	chr2:212066442-212225328	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3459966	chr2:212078710-212080602	Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3459965	chr2:212078798-212080512	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3459967	chr2:212078798-212080512	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv14898	chr2:212078897-212080615	Enhancers	n/a	n/a	inside rSNPs	diseases
9	nsv515773	chr2:212078938-212079450	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212078600-212079000	Enhancers	Rectal Mucosa Donor 29	rectum

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