| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341040-45341453 | Common:4; Rare:192 | ||||
| chr13:45464716-45465018 | Common:1; Rare:74 | ||||
| chr13:46052696-46052834 | Common:2; Rare:38 | ||||
| chr13:48001271-48001405 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:48037610-48037735 | Rare:45 | ||||
| chr13:48533050-48533102 | Rare:17 | ||||
| chr13:48975619-48975928 | Common:2; Rare:94 | ||||
| chr13:49247830-49247964 | Rare:38 | ||||
| chr13:49443993-49444245 | Common:1; Rare:84 | ||||
| chr13:49585471-49585636 | Common:1; Rare:56 | ||||
| chr13:49936260-49936586 | Common:1; Rare:98 | ||||
| chr13:51804144-51804446 | Common:2; Rare:75 | ||||
| chr13:52012136-52012418 | Common:2; Rare:93; Clinvar:1 | ||||
| chr13:52450605-52450730 | Rare:38 | ||||
| chr13:52455335-52455543 | Common:3; Rare:78 |