| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110305563-110305828 | Rare:44 | ||||
| chr13:110306959-110307526 | Common:7; Rare:176; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110462097-110462363 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:110561606-110561918 | Common:5; Rare:108 | ||||
| chr13:110914453-110914540 | Rare:37 | ||||
| chr13:111153619-111153721 | Common:2; Rare:44 | ||||
| chr13:112689783-112690013 | Common:5; Rare:77 | ||||
| chr13:113208630-113208775 | Rare:82 | ||||
| chr13:113297040-113297279 | Common:1; Rare:97 | ||||
| chr13:113364124-113364453 | Common:2; Rare:21 | ||||
| chr13:113490682-113491034 | Common:1; Rare:129 | ||||
| chr13:113863862-113864175 | Common:2; Rare:77 | ||||
| chr13:114281501-114281654 | Common:2; Rare:82 | ||||
| chr14:20343174-20343638 | Common:12; Rare:273 | ||||
| chr14:20413409-20413531 | Common:3; Rare:35 |