| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251247-27251616 | Common:5; Rare:110 | ||||
| chr13:27424499-27424732 | Common:4; Rare:77 | ||||
| chr13:27450130-27450206 | Common:2; Rare:22 | ||||
| chr13:27620469-27620805 | Common:2; Rare:112 | ||||
| chr13:28658942-28659181 | Rare:102; Clinvar (pathogenic):1 | ||||
| chr13:28718797-28719123 | Common:1; Rare:82 | ||||
| chr13:30306845-30306967 | Common:1; Rare:37 | ||||
| chr13:30307001-30307184 | Common:4; Rare:40 | ||||
| chr13:30307404-30307593 | Common:1; Rare:67 | ||||
| chr13:30465795-30466122 | Common:1; Rare:103 | ||||
| chr13:30616979-30617166 | Rare:36 | ||||
| chr13:30617341-30617523 | Rare:56 | ||||
| chr13:30617526-30618019 | Common:1; Rare:160 | ||||
| chr13:31162337-31162455 | Common:1; Rare:31 | ||||
| chr13:32315373-32315553 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):2 |