| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89139930-89140134 | Rare:29 | ||||
| chr15:89168565-89168770 | Rare:29 | ||||
| chr15:89333881-89334155 | Common:1; Rare:63; Clinvar (benign):2 | ||||
| chr15:89358713-89358847 | Common:1; Rare:44 | ||||
| chr15:89362411-89362545 | Rare:48 | ||||
| chr15:89367549-89367742 | Rare:63 | ||||
| chr15:89368007-89368040 | Rare:6 | ||||
| chr15:89399196-89399527 | Common:2; Rare:63 | ||||
| chr15:89400091-89400356 | Common:2; Rare:73 | ||||
| chr15:89400372-89400434 | Common:1; Rare:21 | ||||
| chr15:89407595-89407719 | Rare:20 | ||||
| chr15:89430790-89430906 | Common:1; Rare:28 | ||||
| chr15:89462592-89462831 | Common:3; Rare:65 | ||||
| chr15:90000659-90000727 | Rare:14 | ||||
| chr15:90013536-90013737 | Common:1; Rare:33 |