Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10170124	0.82[ASN][1000 genomes]
rs10176733	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10183135	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10190086	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs10196555	0.82[AFR][1000 genomes]
rs10496137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12713575	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12713578	0.82[ASN][1000 genomes]
rs12713581	0.82[AFR][1000 genomes]
rs12713585	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12713586	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12713587	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12713588	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12995173	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs13009433	0.82[ASN][1000 genomes]
rs13015121	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13020124	0.81[ASN][1000 genomes]
rs1559602	0.81[ASN][1000 genomes]
rs17632177	0.81[ASN][1000 genomes]
rs2113769	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2861285	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35156489	0.81[ASN][1000 genomes]
rs4671755	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6715872	0.81[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	esv2762259	chr2:67109728-67165987	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67141800-67152400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:67145400-67156600	Weak transcription	Fetal Heart	heart
3	chr2:67151000-67152600	Enhancers	Hela-S3	cervix
4	chr2:67151000-67153400	Enhancers	NHEK	skin

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