| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4303252-4303407 | Common:1; Rare:60 | ||||
| chr3:4493172-4493532 | Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979148-4979537 | Common:2; Rare:91 | ||||
| chr3:6862658-6862757 | Common:3; Rare:39 | ||||
| chr3:8501638-8501911 | Common:1; Rare:100 | ||||
| chr3:9249395-9249427 | Rare:6 | ||||
| chr3:9249451-9249743 | Common:1; Rare:67 | ||||
| chr3:9362942-9363098 | Common:2; Rare:57 | ||||
| chr3:9397428-9397688 | Common:1; Rare:98 | ||||
| chr3:9749814-9750050 | Common:1; Rare:75 | ||||
| chr3:9750218-9750320 | Common:1; Rare:48 | ||||
| chr3:9792414-9792518 | Rare:29 | ||||
| chr3:9792685-9793112 | Common:3; Rare:150 | ||||
| chr3:9843975-9844132 | Common:2; Rare:62 | ||||
| chr3:9902679-9902869 | Rare:59 |