Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69087943-69088233 | Rare:63 | ||||
chr10:69179932-69180307 | Common:2; Rare:121 | ||||
chr10:69801581-69801953 | Common:2; Rare:90 | ||||
chr10:70132815-70132878 | Rare:15 | ||||
chr10:70170448-70170722 | Common:3; Rare:86 | ||||
chr10:70233348-70233545 | Common:5; Rare:71 | ||||
chr10:71819597-71819834 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
chr10:72216244-72216496 | Common:2; Rare:76 | ||||
chr10:72354869-72355206 | Common:2; Rare:121 | ||||
chr10:73096906-73097224 | Common:2; Rare:89 | ||||
chr10:73167930-73168141 | Rare:52 | ||||
chr10:73252563-73252796 | Common:2; Rare:67; Clinvar:4; Clinvar (benign):2 | ||||
chr10:73495628-73495771 | Rare:31 | ||||
chr10:73744251-73744442 | Common:1; Rare:51 | ||||
chr10:73772638-73772735 | Rare:56 |