| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50281972-50282197 | Common:2; Rare:79 | ||||
| chr22:50285988-50286235 | Common:1; Rare:84 | ||||
| chr22:50507662-50508018 | Common:1; Rare:85 | ||||
| chr22:50525538-50525685 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50562887-50563055 | Common:3; Rare:46 | ||||
| chr22:50582385-50582467 | Rare:37 | ||||
| chr22:50582784-50583120 | Common:7; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628079-50628276 | Common:9; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50738081-50738236 | Common:2; Rare:36 | ||||
| chr22:50783601-50783859 | Common:2; Rare:79 | ||||
| chr3:197003-197286 | Common:3; Rare:101 | ||||
| chr3:3126806-3126984 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr3:3179673-3179808 | Common:2; Rare:50; Clinvar:1 | ||||
| chr3:4303253-4303405 | Common:1; Rare:58 | ||||
| chr3:4467226-4467277 | Rare:26; Clinvar:1; Clinvar (benign):1 |