| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663490-97663637 | Common:2; Rare:48 | ||||
| chr2:97663880-97664453 | Common:1; Rare:164 | ||||
| chr2:97664487-97664829 | Common:1; Rare:75 | ||||
| chr2:97995142-97995532 | Common:6; Rare:110 | ||||
| chr2:97995796-97995973 | Common:2; Rare:63 | ||||
| chr2:97996103-97996397 | Common:2; Rare:101 | ||||
| chr2:98444700-98444937 | Rare:100 | ||||
| chr2:98608267-98608691 | Common:2; Rare:168; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98609171-98609296 | Common:1; Rare:26 | ||||
| chr2:99141108-99141398 | Common:1; Rare:108 | ||||
| chr2:99154832-99155179 | Common:5; Rare:136; Clinvar (benign):3 | ||||
| chr2:99155448-99155496 | Rare:14 | ||||
| chr2:99180953-99181523 | Common:2; Rare:148 | ||||
| chr2:99336085-99336120 | Rare:9 | ||||
| chr2:99336246-99336635 | Common:2; Rare:113 |