| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507586-74507884 | Common:1; Rare:83 | ||||
| chr2:74508352-74508452 | Rare:23 | ||||
| chr2:74529280-74529441 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr2:74529443-74529524 | Rare:35; Clinvar (benign):1 | ||||
| chr2:74529575-74529911 | Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74530462-74530632 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74548867-74548950 | Rare:27 | ||||
| chr2:74548999-74549146 | Rare:40 | ||||
| chr2:74549665-74549736 | Rare:11 | ||||
| chr2:74552340-74552451 | Rare:26 | ||||
| chr2:74552530-74552848 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr2:74553038-74553089 | Rare:10 | ||||
| chr2:74553106-74553134 | Common:1; Rare:5 | ||||
| chr2:74554643-74554822 | Common:1; Rare:75 | ||||
| chr2:74654062-74654462 | Common:1; Rare:143 |