| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:84716031-84716212 | Rare:55 | ||||
| chr15:84716372-84716529 | Rare:36 | ||||
| chr15:84748265-84748644 | Rare:102 | ||||
| chr15:85380266-85380701 | Common:1; Rare:119 | ||||
| chr15:85543813-85544108 | Common:4; Rare:106 | ||||
| chr15:85681930-85682212 | Common:2; Rare:72 | ||||
| chr15:88467373-88467738 | Common:4; Rare:104 | ||||
| chr15:88546554-88546778 | Rare:78 | ||||
| chr15:88638661-88639092 | Common:1; Rare:121 | ||||
| chr15:89088119-89088530 | Common:5; Rare:98 | ||||
| chr15:89243910-89244042 | Rare:42; Clinvar:3 | ||||
| chr15:89334791-89335069 | Common:3; Rare:104 | ||||
| chr15:89679338-89679540 | Common:1; Rare:35 | ||||
| chr15:89690642-89690806 | Common:2; Rare:49 | ||||
| chr15:89776539-89776825 | Common:3; Rare:121; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):6 |