| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:24954939-24955113 | Rare:90 | ||||
| chr15:25437891-25437973 | Common:1; Rare:23 | ||||
| chr15:25438241-25438636 | Common:2; Rare:120; Clinvar (benign):1 | ||||
| chr15:25438707-25438871 | Rare:50 | ||||
| chr15:25438920-25439307 | Common:3; Rare:137 | ||||
| chr15:28737755-28738095 | Common:3; Rare:118 | ||||
| chr15:29269556-29269966 | Common:5; Rare:183 | ||||
| chr15:29822891-29823036 | Common:1; Rare:37 | ||||
| chr15:29968596-29968705 | Rare:27 | ||||
| chr15:29968850-29969133 | Common:2; Rare:103 | ||||
| chr15:29969140-29969211 | Common:1; Rare:18 | ||||
| chr15:30624357-30624587 | Common:4; Rare:33 | ||||
| chr15:30625646-30625831 | Common:4; Rare:46 | ||||
| chr15:30625977-30626160 | Common:3; Rare:48 | ||||
| chr15:30626809-30626843 | Common:1; Rare:10 |