Variant report

Variant	rs8053662
Chromosome Location	chr16:71543976-71543977
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10500558	0.98[ASN][1000 genomes]
rs11640165	0.98[ASN][1000 genomes]
rs11641492	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11643216	0.98[ASN][1000 genomes]
rs11647749	0.99[ASN][1000 genomes]
rs12446461	0.84[ASN][1000 genomes]
rs13331346	0.91[ASN][1000 genomes]
rs1609868	0.88[ASN][1000 genomes]
rs1609869	0.91[ASN][1000 genomes]
rs2004672	0.96[ASN][1000 genomes]
rs2070832	0.89[ASN][1000 genomes]
rs2288486	0.93[ASN][1000 genomes]
rs2288487	0.90[ASN][1000 genomes]
rs2288488	0.93[ASN][1000 genomes]
rs2303788	0.92[ASN][1000 genomes]
rs28372238	0.98[ASN][1000 genomes]
rs310334	0.96[ASN][1000 genomes]
rs35373081	0.90[ASN][1000 genomes]
rs35916432	0.91[ASN][1000 genomes]
rs3813743	0.92[ASN][1000 genomes]
rs4149498	0.98[ASN][1000 genomes]
rs4503795	0.93[ASN][1000 genomes]
rs58134724	0.93[ASN][1000 genomes]
rs58452291	0.86[ASN][1000 genomes]
rs58719913	0.98[ASN][1000 genomes]
rs59819114	0.83[ASN][1000 genomes]
rs7184543	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7186241	0.99[ASN][1000 genomes]
rs7187165	0.93[ASN][1000 genomes]
rs7187354	0.93[ASN][1000 genomes]
rs7188342	0.93[ASN][1000 genomes]
rs7199026	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7199373	0.93[ASN][1000 genomes]
rs7200335	0.94[ASN][1000 genomes]
rs7200431	0.93[ASN][1000 genomes]
rs7202662	0.99[ASN][1000 genomes]
rs7202953	0.95[ASN][1000 genomes]
rs730470	0.83[ASN][1000 genomes]
rs732318	0.84[ASN][1000 genomes]
rs74026831	0.99[ASN][1000 genomes]
rs74027246	0.98[ASN][1000 genomes]
rs8044068	0.96[ASN][1000 genomes]
rs8044561	0.97[ASN][1000 genomes]
rs8051212	0.93[ASN][1000 genomes]
rs8058294	0.93[ASN][1000 genomes]
rs8058776	0.84[ASN][1000 genomes]
rs8061078	0.86[ASN][1000 genomes]
rs9302623	0.93[ASN][1000 genomes]
rs9926110	0.97[ASN][1000 genomes]
rs9928243	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9933680	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9935426	0.93[ASN][1000 genomes]
rs9936249	0.92[ASN][1000 genomes]
rs9940771	0.88[ASN][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	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv906892	chr16:71526720-71570413	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr16:71543400-71549800	Weak transcription	Pancreas	Pancrea

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