| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:79352387-79352650 | Common:1; Rare:56 | ||||
| chr3:81761494-81761614 | Common:5; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97933566-97933729 | Rare:30 | ||||
| chr3:100045657-100045820 | Rare:28 | ||||
| chr3:100368487-100368645 | Common:1; Rare:30 | ||||
| chr3:100520597-100520832 | Common:2; Rare:45 | ||||
| chr3:100526079-100526215 | Common:1; Rare:22 | ||||
| chr3:101576718-101576863 | Common:1; Rare:26 | ||||
| chr3:101576868-101576973 | Common:1; Rare:30 | ||||
| chr3:101576975-101577085 | Common:1; Rare:31 | ||||
| chr3:101676282-101676474 | Common:1; Rare:63 | ||||
| chr3:101681029-101681156 | Common:2; Rare:27 | ||||
| chr3:107240624-107240762 | Rare:56 | ||||
| chr3:112120401-112120554 | Rare:29 | ||||
| chr3:124751101-124751135 | Rare:7 |