| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110396533-110396566 | Common:1; Rare:4 | ||||
| chr13:110396574-110396747 | Common:1; Rare:28 | ||||
| chr13:110396918-110397339 | Common:2; Rare:59 | ||||
| chr13:110401881-110401888 | Rare:3 | ||||
| chr13:110409538-110409993 | Common:5; Rare:81 | ||||
| chr13:110417654-110417767 | Rare:17 | ||||
| chr13:110419076-110419206 | Rare:25 | ||||
| chr13:110424731-110424995 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110503844-110504264 | Common:4; Rare:140; Clinvar:1; Clinvar (benign):4 | ||||
| chr13:110870249-110870584 | Common:3; Rare:50 | ||||
| chr13:111337209-111337484 | Common:2; Rare:42 | ||||
| chr13:114130972-114131269 | Rare:53 | ||||
| chr13:114131360-114131506 | Common:1; Rare:28 | ||||
| chr14:20625312-20625368 | Common:2; Rare:23 | ||||
| chr14:25091076-25091270 | Rare:30 |