| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:50764086-50764308 | Rare:36 | ||||
| chr15:50764298-50765860 | Common:33; Rare:1249 | ||||
| chr15:50765850-50766130 | Rare:75 | ||||
| chr15:50907915-50908315 | Common:2; Rare:120 | ||||
| chr15:50908443-50908843 | Common:19; Rare:669; Clinvar (benign):13 | ||||
| chr15:50909139-50909403 | Common:2; Rare:64 | ||||
| chr15:51603533-51603970 | Common:3; Rare:161 | ||||
| chr15:51622011-51623192 | Common:22; Rare:1127 | ||||
| chr15:51623147-51623725 | Common:6; Rare:160 | ||||
| chr15:51681250-51681790 | Common:11; Rare:467 | ||||
| chr15:51737520-51737940 | Common:11; Rare:327 | ||||
| chr15:51737978-51738378 | Rare:91 | ||||
| chr15:51750937-51751337 | Common:1; Rare:91 | ||||
| chr15:51751296-51751681 | Common:1; Rare:270 | ||||
| chr15:51751680-51751870 | Rare:43 |