| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100674778-100675061 | Common:3; Rare:116 | ||||
| chr13:102596785-102597035 | Common:1; Rare:119 | ||||
| chr13:102773696-102773896 | Common:1; Rare:85 | ||||
| chr13:102798939-102799201 | Common:1; Rare:54 | ||||
| chr13:102845714-102846167 | Common:9; Rare:116; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567577-106567711 | Rare:48 | ||||
| chr13:106567835-106568278 | Rare:122 | ||||
| chr13:107866955-107867290 | Rare:97 | ||||
| chr13:108215489-108215723 | Common:1; Rare:62 | ||||
| chr13:108218256-108218542 | Common:2; Rare:100 | ||||
| chr13:110561622-110561934 | Common:5; Rare:103 | ||||
| chr13:110615408-110615681 | Common:2; Rare:94 | ||||
| chr13:110712381-110712531 | Rare:72 | ||||
| chr13:110712885-110713266 | Common:2; Rare:179 | ||||
| chr13:110713493-110713657 | Common:2; Rare:70 |