| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:49620763-49621506 | Common:14; Rare:346 | ||||
| chr15:50119220-50119377 | Rare:24 | ||||
| chr15:50181866-50182052 | Common:2; Rare:47 | ||||
| chr15:50182114-50182931 | Common:6; Rare:572 | ||||
| chr15:50182900-50183150 | Common:1; Rare:58 | ||||
| chr15:50354817-50355601 | Common:6; Rare:539 | ||||
| chr15:50424104-50424575 | Common:6; Rare:305 | ||||
| chr15:50686534-50686941 | Common:9; Rare:218 | ||||
| chr15:50765113-50765533 | Common:4; Rare:206 | ||||
| chr15:50765551-50765769 | Common:4; Rare:144 | ||||
| chr15:50908050-50908450 | Common:1; Rare:186 | ||||
| chr15:50908507-50908781 | Common:6; Rare:214; Clinvar (benign):5 | ||||
| chr15:51622666-51623210 | Common:6; Rare:327 | ||||
| chr15:51737615-51737730 | Common:1; Rare:42 | ||||
| chr15:51829546-51829828 | Common:2; Rare:150 |