| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:48810930-48811421 | Common:8; Rare:230; Clinvar:8; Clinvar (benign):8 | ||||
| chr15:48877940-48878572 | Common:1; Rare:480 | ||||
| chr15:48962939-48963269 | Common:2; Rare:103 | ||||
| chr15:48963281-48963861 | Common:4; Rare:174 | ||||
| chr15:48963795-48964084 | Rare:101 | ||||
| chr15:49046290-49046850 | Common:4; Rare:276 | ||||
| chr15:49155511-49155844 | Common:6; Rare:307 | ||||
| chr15:49169943-49170690 | Common:2; Rare:286 | ||||
| chr15:49620715-49621194 | Common:22; Rare:423 | ||||
| chr15:50182054-50182457 | Common:2; Rare:185 | ||||
| chr15:50182466-50183310 | Common:8; Rare:571 | ||||
| chr15:50354389-50355942 | Common:18; Rare:1218 | ||||
| chr15:50423947-50424664 | Common:9; Rare:559 | ||||
| chr15:50686458-50687015 | Common:16; Rare:456 | ||||
| chr15:50765189-50765884 | Common:13; Rare:506 |