Variant report

Variant	rs35916432
Chromosome Location	chr16:71553242-71553243
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10500558	0.93[ASN][1000 genomes]
rs11640165	0.93[ASN][1000 genomes]
rs11641492	0.93[ASN][1000 genomes]
rs11643216	0.93[ASN][1000 genomes]
rs11647749	0.92[ASN][1000 genomes]
rs13331346	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1609868	0.81[ASN][1000 genomes]
rs1609869	0.84[ASN][1000 genomes]
rs2004672	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2070832	0.82[ASN][1000 genomes]
rs2288486	0.88[ASN][1000 genomes]
rs2288487	0.84[ASN][1000 genomes]
rs2288488	0.88[ASN][1000 genomes]
rs2303788	0.90[ASN][1000 genomes]
rs28372238	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs310334	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35373081	0.85[ASN][1000 genomes]
rs3813743	0.88[ASN][1000 genomes]
rs4149498	0.93[ASN][1000 genomes]
rs4503795	0.87[ASN][1000 genomes]
rs4620964	0.82[AMR][1000 genomes]
rs58134724	0.86[ASN][1000 genomes]
rs58452291	0.81[ASN][1000 genomes]
rs58719913	0.93[ASN][1000 genomes]
rs7184543	0.92[ASN][1000 genomes]
rs7186241	0.92[ASN][1000 genomes]
rs7187165	0.86[ASN][1000 genomes]
rs7187354	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7188342	0.86[ASN][1000 genomes]
rs7199026	0.92[ASN][1000 genomes]
rs7199373	0.86[ASN][1000 genomes]
rs7200335	0.89[ASN][1000 genomes]
rs7200431	0.86[ASN][1000 genomes]
rs7202662	0.92[ASN][1000 genomes]
rs7202953	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs74026831	0.92[ASN][1000 genomes]
rs74027246	0.93[ASN][1000 genomes]
rs8044068	0.94[ASN][1000 genomes]
rs8044561	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8051212	0.89[ASN][1000 genomes]
rs8053662	0.91[ASN][1000 genomes]
rs8058294	0.86[ASN][1000 genomes]
rs8061078	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9302623	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9926110	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9928243	0.92[ASN][1000 genomes]
rs9933680	0.91[ASN][1000 genomes]
rs9935426	0.86[ASN][1000 genomes]
rs9936249	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9940771	0.85[AMR][1000 genomes];0.84[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71549200-71558400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr16:71551200-71554400	Weak transcription	Pancreas	Pancrea

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