| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:71866287-71866564 | Common:4; Rare:120; Clinvar:1 | ||||
| chr13:71867190-71867357 | Common:1; Rare:43 | ||||
| chr13:71867361-71867481 | Rare:30 | ||||
| chr13:72727551-72727981 | Common:7; Rare:174 | ||||
| chr13:72781673-72782273 | Common:2; Rare:212 | ||||
| chr13:74133756-74133954 | Common:3; Rare:48 | ||||
| chr13:74134096-74134378 | Common:2; Rare:93 | ||||
| chr13:75537786-75538144 | Common:3; Rare:113 | ||||
| chr13:75549352-75549831 | Common:9; Rare:128 | ||||
| chr13:76991949-76992199 | Common:4; Rare:119; Clinvar:21; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr13:77027137-77027310 | Common:6; Rare:59 | ||||
| chr13:77326180-77326209 | Rare:4 | ||||
| chr13:77326577-77326822 | Common:1; Rare:72 | ||||
| chr13:77327054-77327380 | Common:1; Rare:111 | ||||
| chr13:78659053-78659242 | Common:2; Rare:130 |