| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72727604-72727950 | Common:4; Rare:124 | ||||
| chr13:72781896-72782188 | Common:1; Rare:111 | ||||
| chr13:94601550-94601918 | Common:4; Rare:110 | ||||
| chr13:95676887-95677182 | Common:3; Rare:111 | ||||
| chr13:99200672-99200894 | Common:6; Rare:102 | ||||
| chr13:100088955-100089117 | Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100674814-100675060 | Common:3; Rare:101 | ||||
| chr13:102596804-102597028 | Common:1; Rare:106 | ||||
| chr13:108218294-108218520 | Common:1; Rare:84 | ||||
| chr13:112969135-112969337 | Common:2; Rare:57 | ||||
| chr13:113208641-113208743 | Rare:56 | ||||
| chr13:113490699-113490878 | Rare:61 | ||||
| chr13:114281787-114282065 | Common:6; Rare:145 | ||||
| chr14:20343199-20343635 | Common:12; Rare:257 | ||||
| chr14:20413456-20413531 | Common:3; Rare:24 |