Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70602708-70602852 | Common:1; Rare:18; Clinvar:1 | ||||
chr10:71773426-71773751 | Common:4; Rare:97 | ||||
chr10:72273701-72273947 | Rare:67 | ||||
chr10:73096804-73097024 | Common:3; Rare:68 | ||||
chr10:73167913-73168142 | Rare:57 | ||||
chr10:73252556-73252807 | Common:2; Rare:74; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495595-73495771 | Rare:38 | ||||
chr10:73495818-73496130 | Common:2; Rare:88 | ||||
chr10:73625962-73626118 | Rare:29 | ||||
chr10:73744251-73744430 | Common:1; Rare:47 | ||||
chr10:73772669-73772708 | Rare:20 | ||||
chr10:73782000-73782084 | Common:1; Rare:28 | ||||
chr10:73997854-73998375 | Common:1; Rare:139; Clinvar:4; Clinvar (benign):4 | ||||
chr10:74151053-74151281 | Common:1; Rare:72 | ||||
chr10:74176410-74176558 | Rare:36 |