| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27424432-27424818 | Common:5; Rare:130 | ||||
| chr13:27450130-27450212 | Common:2; Rare:23 | ||||
| chr13:27450515-27450643 | Common:2; Rare:57 | ||||
| chr13:28658864-28659210 | Common:2; Rare:130; Clinvar (pathogenic):1 | ||||
| chr13:30465885-30465977 | Rare:30 | ||||
| chr13:30616953-30617102 | Rare:27 | ||||
| chr13:30735386-30735602 | Common:2; Rare:46 | ||||
| chr13:32031554-32031785 | Common:1; Rare:65 | ||||
| chr13:32538712-32538993 | Common:1; Rare:71 | ||||
| chr13:36346303-36346453 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:39038053-39038495 | Common:1; Rare:107 | ||||
| chr13:40666604-40666805 | Common:2; Rare:65 | ||||
| chr13:40771145-40771444 | Common:3; Rare:84 | ||||
| chr13:40982859-40983029 | Common:3; Rare:27 | ||||
| chr13:41061172-41061569 | Common:3; Rare:138 |