| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119294245-119294382 | Rare:29 | ||||
| chr3:119463590-119463780 | Common:4; Rare:56 | ||||
| chr3:119468834-119469024 | Common:1; Rare:74 | ||||
| chr3:119498341-119498609 | Common:4; Rare:93 | ||||
| chr3:119677306-119677505 | Common:1; Rare:73 | ||||
| chr3:120094436-120094756 | Common:3; Rare:99 | ||||
| chr3:120450930-120451320 | Rare:126 | ||||
| chr3:120596137-120596458 | Common:2; Rare:125 | ||||
| chr3:120742490-120742793 | Common:2; Rare:89 | ||||
| chr3:120908066-120908248 | Rare:54 | ||||
| chr3:121545962-121546089 | Common:1; Rare:34 | ||||
| chr3:121660885-121661009 | Rare:17 | ||||
| chr3:121749142-121749293 | Rare:27 | ||||
| chr3:121749643-121750021 | Common:1; Rare:87 | ||||
| chr3:121834972-121835244 | Common:3; Rare:89; Clinvar:6; Clinvar (benign):2 |