| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112254810-112255228 | Common:3; Rare:153 | ||||
| chr2:112275220-112275762 | Common:1; Rare:181 | ||||
| chr2:112275803-112276364 | Rare:166 | ||||
| chr2:112481908-112482191 | Common:1; Rare:97 | ||||
| chr2:112541350-112541486 | Rare:30 | ||||
| chr2:112541759-112541933 | Common:1; Rare:41 | ||||
| chr2:112541995-112542258 | Rare:63 | ||||
| chr2:112542262-112542547 | Common:2; Rare:101 | ||||
| chr2:112542885-112542979 | Rare:12 | ||||
| chr2:112584265-112585012 | Common:3; Rare:196 | ||||
| chr2:112645252-112645435 | Rare:42 | ||||
| chr2:112645488-112646057 | Common:3; Rare:182 | ||||
| chr2:112646229-112646406 | Common:2; Rare:59 | ||||
| chr2:112764092-112764281 | Common:1; Rare:58 | ||||
| chr2:112764547-112765046 | Common:8; Rare:168; Clinvar (pathogenic):1 |