| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133181359-133181553 | Common:2; Rare:59 | ||||
| chr13:19633531-19633774 | Common:1; Rare:91 | ||||
| chr13:19782912-19783090 | Common:2; Rare:64 | ||||
| chr13:19863538-19863866 | Common:5; Rare:121 | ||||
| chr13:20525796-20525962 | Common:1; Rare:65 | ||||
| chr13:21140360-21140639 | Rare:124 | ||||
| chr13:21176405-21176708 | Common:2; Rare:132 | ||||
| chr13:21459167-21459526 | Common:1; Rare:130 | ||||
| chr13:21604036-21604236 | Common:5; Rare:108 | ||||
| chr13:21670902-21671170 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23570300-23570489 | Common:1; Rare:38 | ||||
| chr13:23579265-23579456 | Common:3; Rare:61 | ||||
| chr13:23889298-23889591 | Common:1; Rare:103 | ||||
| chr13:24160562-24160780 | Rare:64 | ||||
| chr13:24270646-24270785 | Common:2; Rare:31 |