| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50525543-50525712 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50532140-50532329 | Common:1; Rare:48 | ||||
| chr22:50532494-50532639 | Common:2; Rare:38 | ||||
| chr22:50562881-50563055 | Common:3; Rare:47 | ||||
| chr22:50578394-50578712 | Common:1; Rare:85 | ||||
| chr22:50582391-50582467 | Rare:33 | ||||
| chr22:50582605-50582696 | Rare:37; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50582777-50583142 | Common:7; Rare:124; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628026-50628276 | Common:9; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783587-50783877 | Common:2; Rare:96 | ||||
| chr3:197196-197332 | Rare:44 | ||||
| chr3:1092970-1093058 | Common:1; Rare:18 | ||||
| chr3:2098649-2098962 | Common:4; Rare:125 | ||||
| chr3:3126813-3126990 | Common:4; Rare:78; Clinvar (benign):2 | ||||
| chr3:3800761-3800911 | Rare:34 |