| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46250263-46250423 | Common:3; Rare:53 | ||||
| chr22:46296760-46296915 | Rare:52 | ||||
| chr22:46335621-46335778 | Common:4; Rare:66; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46762512-46762688 | Common:3; Rare:61 | ||||
| chr22:49853592-49853915 | Common:2; Rare:117 | ||||
| chr22:50525538-50525661 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783565-50783859 | Common:2; Rare:99 | ||||
| chr3:196536-196614 | Rare:18 | ||||
| chr3:196707-197054 | Common:2; Rare:112 | ||||
| chr3:197223-197335 | Rare:36 | ||||
| chr3:197503-198038 | Common:7; Rare:196 | ||||
| chr3:2098651-2098962 | Common:4; Rare:123 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr3:4493177-4493350 | Rare:61 | ||||
| chr3:6862658-6862784 | Common:3; Rare:46 |