| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3261490-3261584 | Common:1; Rare:28 | ||||
| chr18:3261610-3261878 | Common:4; Rare:67 | ||||
| chr18:3261924-3262268 | Common:4; Rare:110 | ||||
| chr18:3262697-3262754 | Rare:16 | ||||
| chr18:3262977-3263069 | Rare:14 | ||||
| chr18:3447547-3447651 | Rare:27 | ||||
| chr18:3447941-3448558 | Common:7; Rare:161 | ||||
| chr18:3448888-3449094 | Common:2; Rare:30 | ||||
| chr18:3449102-3449259 | Common:1; Rare:35 | ||||
| chr18:3449288-3449389 | Common:3; Rare:27 | ||||
| chr18:3449394-3449666 | Common:2; Rare:73 | ||||
| chr18:3449999-3450455 | Common:1; Rare:124; Clinvar (benign):1 | ||||
| chr18:3450475-3450542 | Rare:29 | ||||
| chr18:3451203-3451628 | Common:2; Rare:100 | ||||
| chr18:3451633-3451792 | Common:3; Rare:35 |