| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41263472-41263621 | Rare:36 | ||||
| chr13:41311032-41311366 | Common:3; Rare:119 | ||||
| chr13:41457385-41457583 | Common:2; Rare:66 | ||||
| chr13:41463911-41464091 | Common:1; Rare:29 | ||||
| chr13:41960368-41960657 | Common:2; Rare:50 | ||||
| chr13:41960820-41960886 | Common:1; Rare:14 | ||||
| chr13:41960974-41961356 | Common:4; Rare:116 | ||||
| chr13:42039789-42040077 | Common:1; Rare:59 | ||||
| chr13:42040278-42040645 | Common:2; Rare:114 | ||||
| chr13:42048869-42049273 | Common:3; Rare:87 | ||||
| chr13:42271632-42272211 | Common:6; Rare:146 | ||||
| chr13:42272357-42272474 | Common:1; Rare:33 | ||||
| chr13:42574006-42574180 | Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:42574189-42574283 | Rare:29; Clinvar:3 | ||||
| chr13:42991809-42991894 | Rare:18 |