| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:73000046-73000446 | Common:8; Rare:97 | ||||
| chr13:73961132-73961532 | Common:4; Rare:75 | ||||
| chr13:74026770-74027060 | Common:1; Rare:105 | ||||
| chr13:74027546-74027765 | Rare:30 | ||||
| chr13:74062233-74062633 | Common:2; Rare:78 | ||||
| chr13:74063092-74063320 | Rare:30 | ||||
| chr13:74135368-74135738 | Common:6; Rare:215 | ||||
| chr13:74135792-74135919 | Common:1; Rare:29 | ||||
| chr13:74157928-74158328 | Common:4; Rare:160 | ||||
| chr13:75091645-75092045 | Common:3; Rare:122 | ||||
| chr13:75219731-75220131 | Common:4; Rare:135 | ||||
| chr13:75299199-75299861 | Common:4; Rare:148; Clinvar (pathogenic):1 | ||||
| chr13:75299869-75300339 | Common:2; Rare:96 | ||||
| chr13:75300317-75300446 | Common:3; Rare:22 | ||||
| chr13:75308404-75308507 | Rare:20 |