| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:98899481-98899981 | Common:2; Rare:139; Clinvar:1 | ||||
| chr15:98901580-98901713 | Rare:30 | ||||
| chr15:98901727-98901991 | Common:2; Rare:58 | ||||
| chr15:99258547-99258751 | Common:1; Rare:35 | ||||
| chr15:99259228-99259295 | Common:1; Rare:7 | ||||
| chr15:99297204-99297412 | Common:2; Rare:27 | ||||
| chr15:99430933-99431043 | Common:1; Rare:31 | ||||
| chr15:99610294-99610413 | Rare:24 | ||||
| chr15:100398869-100399088 | Common:6; Rare:33 | ||||
| chr15:100713451-100713515 | Common:1; Rare:13 | ||||
| chr15:100721668-100721931 | Common:2; Rare:60 | ||||
| chr15:100723486-100723713 | Common:3; Rare:40 | ||||
| chr15:100885266-100885639 | Common:3; Rare:77; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:100887411-100887713 | Common:2; Rare:73; Clinvar (pathogenic):2 | ||||
| chr15:100892791-100893009 | Common:3; Rare:40 |