| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71454445-71454737 | Rare:57 | ||||
| chr2:71513326-71513396 | Rare:21 | ||||
| chr2:71535053-71535311 | Common:5; Rare:68; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr2:71539054-71539195 | Common:1; Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:71539269-71539437 | Common:3; Rare:33 | ||||
| chr2:73700138-73700504 | Common:1; Rare:80 | ||||
| chr2:73728144-73728341 | Common:3; Rare:50 | ||||
| chr2:73983268-73983587 | Common:2; Rare:60 | ||||
| chr2:74120115-74120409 | Common:2; Rare:94 | ||||
| chr2:74120562-74120594 | Common:1; Rare:8 | ||||
| chr2:74159193-74159299 | Rare:27 | ||||
| chr2:74370474-74370820 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:74377432-74377690 | Common:1; Rare:65 | ||||
| chr2:74534716-74534977 | Common:1; Rare:79 | ||||
| chr2:75667692-75667929 | Common:1; Rare:52 |