| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:50546600-50546787 | Rare:36 | ||||
| chr15:50582451-50582527 | Common:2; Rare:12 | ||||
| chr15:50686715-50686939 | Common:5; Rare:92 | ||||
| chr15:50765529-50765785 | Common:2; Rare:89 | ||||
| chr15:50908188-50908322 | Rare:39 | ||||
| chr15:50908595-50908790 | Common:1; Rare:82; Clinvar (benign):3 | ||||
| chr15:51622757-51623171 | Common:3; Rare:137 | ||||
| chr15:51738099-51738216 | Rare:24 | ||||
| chr15:51751465-51751694 | Common:1; Rare:57 | ||||
| chr15:51829571-51829751 | Common:1; Rare:60 | ||||
| chr15:51971396-51971513 | Common:1; Rare:28 | ||||
| chr15:51971667-51971862 | Rare:87 | ||||
| chr15:52019073-52019294 | Common:1; Rare:115 | ||||
| chr15:52179668-52180057 | Common:1; Rare:134 | ||||
| chr15:52568855-52568941 | Rare:40 |