| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:107867058-107867154 | Rare:25 | ||||
| chr13:108218293-108218520 | Common:1; Rare:84 | ||||
| chr13:110305638-110305750 | Rare:14 | ||||
| chr13:110306954-110307526 | Common:7; Rare:177; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110713008-110713261 | Common:2; Rare:111 | ||||
| chr13:110715831-110715839 | Rare:3 | ||||
| chr13:111153622-111153714 | Common:2; Rare:40 | ||||
| chr13:113208641-113208762 | Rare:64 | ||||
| chr13:113863832-113864180 | Common:3; Rare:85 | ||||
| chr13:114281480-114281684 | Common:2; Rare:112 | ||||
| chr14:20343167-20343644 | Common:13; Rare:280 | ||||
| chr14:20413422-20413763 | Common:4; Rare:74 | ||||
| chr14:20454893-20455245 | Common:3; Rare:90 | ||||
| chr14:20684470-20684629 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr14:21025037-21025234 | Rare:71 |