| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:2098605-2098962 | Common:4; Rare:142 | ||||
| chr3:3126778-3126997 | Common:4; Rare:96; Clinvar (benign):2 | ||||
| chr3:4303279-4303407 | Common:1; Rare:55 | ||||
| chr3:4493165-4493359 | Rare:73; Clinvar:1 | ||||
| chr3:6862653-6862784 | Common:3; Rare:49 | ||||
| chr3:8501644-8501854 | Rare:73 | ||||
| chr3:9249592-9249750 | Common:1; Rare:37 | ||||
| chr3:9362948-9363098 | Common:2; Rare:54 | ||||
| chr3:9397434-9397688 | Common:1; Rare:94 | ||||
| chr3:9749773-9750018 | Common:1; Rare:84 | ||||
| chr3:9750029-9750320 | Common:1; Rare:87 | ||||
| chr3:9792380-9792499 | Rare:34 | ||||
| chr3:9792691-9793119 | Common:3; Rare:150 | ||||
| chr3:9843986-9844128 | Common:2; Rare:51 | ||||
| chr3:9890474-9890667 | Common:2; Rare:72 |