| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50611737-50611883 | Rare:34 | ||||
| chr3:51385025-51385345 | Common:2; Rare:97 | ||||
| chr3:51975048-51975143 | Common:1; Rare:35 | ||||
| chr3:51983395-51983548 | Rare:36 | ||||
| chr3:52239041-52239255 | Common:2; Rare:74 | ||||
| chr3:52278625-52278791 | Rare:58 | ||||
| chr3:52288005-52288075 | Rare:26 | ||||
| chr3:52451743-52452260 | Rare:130; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr3:52455303-52455644 | Common:2; Rare:95 | ||||
| chr3:52495282-52495398 | Common:1; Rare:32 | ||||
| chr3:52685593-52685802 | Common:2; Rare:50 | ||||
| chr3:52685926-52686052 | Common:1; Rare:44 | ||||
| chr3:52705576-52706188 | Common:4; Rare:195 | ||||
| chr3:53130398-53130545 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53891794-53892002 | Common:2; Rare:67 |