| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:60397325-60398010 | Common:7; Rare:251 | ||||
| chr13:67230242-67230785 | Common:2; Rare:170 | ||||
| chr13:67230833-67230940 | Common:1; Rare:25 | ||||
| chr13:72727209-72727371 | Common:5; Rare:36 | ||||
| chr13:72727547-72727981 | Common:7; Rare:175 | ||||
| chr13:72781350-72781382 | Rare:7 | ||||
| chr13:72781585-72781799 | Common:1; Rare:80 | ||||
| chr13:72781807-72782302 | Common:1; Rare:173 | ||||
| chr13:73058536-73059244 | Common:2; Rare:237 | ||||
| chr13:73060292-73060442 | Common:1; Rare:40 | ||||
| chr13:73060947-73061139 | Rare:43 | ||||
| chr13:74133896-74133929 | Rare:10 | ||||
| chr13:74133986-74134112 | Common:1; Rare:32 | ||||
| chr13:74134246-74134672 | Common:5; Rare:154 | ||||
| chr13:75481666-75482113 | Common:3; Rare:124; Clinvar (benign):1 |