| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:73337663-73337907 | Rare:47 | ||||
| chr13:73338470-73338696 | Rare:43 | ||||
| chr13:73368648-73368976 | Rare:57 | ||||
| chr13:73369050-73369194 | Common:1; Rare:29 | ||||
| chr13:73423043-73423344 | Common:3; Rare:47 | ||||
| chr13:73428250-73428307 | Rare:6 | ||||
| chr13:73429794-73429996 | Common:1; Rare:39 | ||||
| chr13:73497485-73497797 | Rare:46 | ||||
| chr13:73585366-73585496 | Common:2; Rare:22 | ||||
| chr13:73610683-73611054 | Common:2; Rare:63 | ||||
| chr13:73934604-73934919 | Common:4; Rare:44 | ||||
| chr13:74089566-74089798 | Common:2; Rare:33 | ||||
| chr13:74122793-74122952 | Rare:28 | ||||
| chr13:75310036-75310247 | Common:2; Rare:60; Clinvar (benign):2 | ||||
| chr13:75482619-75482672 | Common:1; Rare:7 |