Variant report

Variant	rs9716322
Chromosome Location	chr5:112750674-112750675
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10038521	0.83[ASN][1000 genomes]
rs10051115	0.83[ASN][1000 genomes]
rs10053341	0.83[ASN][1000 genomes]
rs10061462	0.83[ASN][1000 genomes]
rs10477490	0.83[ASN][1000 genomes]
rs13154300	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13159509	0.87[ASN][1000 genomes]
rs13171482	0.83[ASN][1000 genomes]
rs13174075	0.83[ASN][1000 genomes]
rs13174206	0.87[ASN][1000 genomes]
rs13180516	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13180522	0.83[ASN][1000 genomes]
rs13181534	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13181732	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13181944	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13183383	0.82[ASN][1000 genomes]
rs13187823	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13189050	0.83[ASN][1000 genomes]
rs13189910	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17327964	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17388260	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs17389165	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs34316732	0.83[ASN][1000 genomes]
rs34682492	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34951736	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35359071	0.87[ASN][1000 genomes]
rs35886114	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4438866	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56180725	0.81[EUR][1000 genomes]
rs6594706	0.83[ASN][1000 genomes]
rs6594713	0.83[ASN][1000 genomes]
rs6594714	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6594715	0.83[ASN][1000 genomes]
rs6594716	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs66572866	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs67320720	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs67693032	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6870401	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6871934	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6872490	0.83[ASN][1000 genomes]
rs6883102	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6887482	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6887914	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6889489	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6890874	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6896843	0.87[ASN][1000 genomes]
rs71577447	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71577448	0.87[ASN][1000 genomes]
rs7709646	0.82[ASN][1000 genomes]
rs7714221	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7714760	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7717630	0.83[ASN][1000 genomes]
rs7718616	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7725712	0.83[ASN][1000 genomes]
rs7729269	0.83[ASN][1000 genomes]
rs7731231	0.83[ASN][1000 genomes]
rs7734576	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599396	chr5:112408944-112853189	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr5:112724400-112751200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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