| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46335758-46335927 | Rare:35 | ||||
| chr2:46335936-46336267 | Common:1; Rare:69 | ||||
| chr2:46541883-46542036 | Common:3; Rare:33 | ||||
| chr2:46542367-46542433 | Rare:14 | ||||
| chr2:46542507-46542760 | Rare:83 | ||||
| chr2:46616670-46616733 | Rare:14 | ||||
| chr2:46616833-46617315 | Common:11; Rare:186; Clinvar (pathogenic):1 | ||||
| chr2:46698311-46698605 | Common:4; Rare:64 | ||||
| chr2:46698647-46699461 | Common:5; Rare:237 | ||||
| chr2:46699483-46699657 | Common:2; Rare:60 | ||||
| chr2:46915581-46916233 | Common:6; Rare:212; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916305-46916386 | Common:2; Rare:20 | ||||
| chr2:46940699-46940947 | Common:3; Rare:63 | ||||
| chr2:46941004-46941332 | Common:2; Rare:121 | ||||
| chr2:46941428-46941906 | Common:6; Rare:158; Clinvar:2; Clinvar (benign):3 |