| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73828730-73829037 | Common:1; Rare:68 | ||||
| chr2:73829500-73829542 | Rare:9 | ||||
| chr2:73926689-73927017 | Common:2; Rare:153; Clinvar:10; Clinvar (benign):3 | ||||
| chr2:73927066-73927139 | Rare:17 | ||||
| chr2:73985837-73985981 | Common:1; Rare:28 | ||||
| chr2:74002531-74002723 | Common:2; Rare:75 | ||||
| chr2:74147806-74148162 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:74178193-74178511 | Rare:55 | ||||
| chr2:74178713-74179104 | Common:6; Rare:118 | ||||
| chr2:74198312-74198703 | Common:5; Rare:148 | ||||
| chr2:74199042-74199363 | Common:1; Rare:67 | ||||
| chr2:74206461-74206634 | Common:1; Rare:41 | ||||
| chr2:74391793-74392182 | Common:2; Rare:173 | ||||
| chr2:74421274-74421385 | Common:1; Rare:11 | ||||
| chr2:74421487-74421803 | Rare:96 |