| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74503307-74503501 | Rare:52 | ||||
| chr2:74507221-74507533 | Common:2; Rare:83 | ||||
| chr2:74507592-74507823 | Rare:58 | ||||
| chr2:74529601-74530020 | Rare:138; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:74530434-74530638 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74548933-74549133 | Rare:55 | ||||
| chr2:74553926-74554107 | Rare:33 | ||||
| chr2:74555624-74555906 | Common:1; Rare:80 | ||||
| chr2:74577067-74577074 | Rare:1 | ||||
| chr2:74654113-74654364 | Rare:86 | ||||
| chr2:74833823-74834227 | Common:1; Rare:122 | ||||
| chr2:74835133-74835324 | Rare:49 | ||||
| chr2:74958560-74958701 | Common:3; Rare:53 | ||||
| chr2:74958872-74959038 | Rare:62 | ||||
| chr2:75646992-75647064 | Common:1; Rare:14 |