| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:45567501-45567733 | Rare:53 | ||||
| chr2:45568048-45568374 | Common:1; Rare:66 | ||||
| chr2:45611134-45611411 | Rare:97 | ||||
| chr2:45650953-45651284 | Common:3; Rare:95 | ||||
| chr2:45651373-45651382 | |||||
| chr2:46073674-46073734 | Common:1; Rare:11 | ||||
| chr2:46541955-46542107 | Common:2; Rare:33 | ||||
| chr2:46542273-46542769 | Common:1; Rare:144 | ||||
| chr2:46543275-46543414 | Rare:32 | ||||
| chr2:46616238-46616318 | Rare:14 | ||||
| chr2:46616932-46617321 | Common:11; Rare:157; Clinvar (pathogenic):1 | ||||
| chr2:46698416-46698603 | Common:2; Rare:45 | ||||
| chr2:46698668-46699372 | Common:3; Rare:213 | ||||
| chr2:46915690-46916085 | Common:3; Rare:134; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916101-46916238 | Rare:37 |