| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31292360-31292951 | Common:2; Rare:157 | ||||
| chr22:31345213-31345634 | Rare:204 | ||||
| chr22:31345720-31346200 | Common:7; Rare:271 | ||||
| chr22:31346302-31346898 | Common:13; Rare:240 | ||||
| chr22:31399335-31399681 | Common:3; Rare:192 | ||||
| chr22:31489693-31490203 | Common:4; Rare:283 | ||||
| chr22:31495940-31496289 | Common:2; Rare:137 | ||||
| chr22:31496373-31496589 | Common:3; Rare:93 | ||||
| chr22:31630799-31631068 | Common:11; Rare:113 | ||||
| chr22:31662171-31662377 | Common:4; Rare:158 | ||||
| chr22:31749961-31750343 | Common:6; Rare:185 | ||||
| chr22:31753749-31754152 | Common:2; Rare:270 | ||||
| chr22:31944279-31944710 | Common:12; Rare:289 | ||||
| chr22:32412136-32412325 | Common:4; Rare:108 | ||||
| chr22:32474595-32475118 | Common:8; Rare:241; Clinvar:10; Clinvar (benign):4 |