| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:78944970-78945234 | Common:18; Rare:233 | ||||
| chr15:79090182-79090443 | Common:1; Rare:85 | ||||
| chr15:79090635-79090873 | Rare:70 | ||||
| chr15:79310746-79311358 | Common:15; Rare:392 | ||||
| chr15:79432751-79432855 | Common:2; Rare:25 | ||||
| chr15:79896580-79896914 | Common:21; Rare:294; Clinvar (pathogenic):1 | ||||
| chr15:79896901-79897231 | Common:10; Rare:279 | ||||
| chr15:79897240-79897640 | Common:5; Rare:120 | ||||
| chr15:79922950-79923283 | Common:7; Rare:328 | ||||
| chr15:79923502-79924141 | Common:26; Rare:569 | ||||
| chr15:80059340-80059795 | Common:3; Rare:383 | ||||
| chr15:80059797-80060063 | Common:2; Rare:158 | ||||
| chr15:80060106-80061728 | Common:16; Rare:578 | ||||
| chr15:80152292-80153044 | Common:20; Rare:155; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:80152997-80153176 | Common:4; Rare:56; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 |