| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100674767-100675161 | Common:4; Rare:162 | ||||
| chr13:101416360-101416515 | Rare:37 | ||||
| chr13:102402236-102402466 | Rare:39 | ||||
| chr13:102596773-102597039 | Common:1; Rare:122 | ||||
| chr13:102773716-102773896 | Common:1; Rare:79 | ||||
| chr13:102798899-102799180 | Common:1; Rare:59 | ||||
| chr13:102845719-102846172 | Common:9; Rare:115; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567587-106567705 | Rare:45 | ||||
| chr13:106567841-106568285 | Rare:122 | ||||
| chr13:107866144-107866285 | Rare:62 | ||||
| chr13:107866946-107867112 | Rare:34 | ||||
| chr13:108215502-108215746 | Common:1; Rare:64 | ||||
| chr13:108218237-108218633 | Common:2; Rare:140 | ||||
| chr13:110615507-110615656 | Rare:55 | ||||
| chr13:110712353-110712563 | Rare:99 |