| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:50765894-50766142 | Rare:45 | ||||
| chr15:50908234-50908829 | Common:8; Rare:447; Clinvar (benign):10 | ||||
| chr15:51341240-51341753 | Common:11; Rare:222 | ||||
| chr15:51622568-51623185 | Common:9; Rare:451 | ||||
| chr15:51737549-51737901 | Common:5; Rare:189 | ||||
| chr15:51737936-51738310 | Rare:115 | ||||
| chr15:51751111-51751367 | Common:1; Rare:109 | ||||
| chr15:51751372-51751685 | Common:1; Rare:162 | ||||
| chr15:51829482-51829848 | Common:2; Rare:150 | ||||
| chr15:51934398-51934498 | Rare:13 | ||||
| chr15:51971218-51971572 | Common:3; Rare:123 | ||||
| chr15:51971646-51972133 | Common:5; Rare:338 | ||||
| chr15:52019018-52019996 | Common:22; Rare:888 | ||||
| chr15:52111990-52112370 | Common:3; Rare:100 | ||||
| chr15:52179226-52179571 | Common:8; Rare:126 |