| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26221791-26222001 | Rare:64 | ||||
| chr13:26222190-26222365 | Common:3; Rare:47 | ||||
| chr13:27251258-27251632 | Common:4; Rare:111 | ||||
| chr13:27424507-27424821 | Common:3; Rare:103 | ||||
| chr13:27450119-27450222 | Common:3; Rare:32 | ||||
| chr13:27620465-27620810 | Common:2; Rare:117 | ||||
| chr13:28658948-28658992 | Rare:10 | ||||
| chr13:28659055-28659184 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr13:30307001-30307197 | Common:4; Rare:46 | ||||
| chr13:30465767-30466119 | Common:1; Rare:108 | ||||
| chr13:30617577-30618000 | Common:1; Rare:129 | ||||
| chr13:32315384-32315552 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32538681-32538943 | Common:1; Rare:74 | ||||
| chr13:33285710-33285880 | Rare:38 | ||||
| chr13:33818015-33818197 | Common:1; Rare:79 |