| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53891794-53892030 | Common:2; Rare:71 | ||||
| chr3:56557086-56557232 | Common:2; Rare:57 | ||||
| chr3:56682990-56683370 | Common:4; Rare:130 | ||||
| chr3:56801914-56802024 | Rare:40 | ||||
| chr3:57079233-57079382 | Common:2; Rare:50 | ||||
| chr3:57227600-57227922 | Common:4; Rare:107 | ||||
| chr3:57555996-57556322 | Rare:81 | ||||
| chr3:57597286-57597778 | Common:4; Rare:146 | ||||
| chr3:58237423-58237816 | Common:10; Rare:110 | ||||
| chr3:58433794-58434019 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58526764-58526864 | Rare:9 | ||||
| chr3:61251383-61251593 | Common:4; Rare:53 | ||||
| chr3:61561412-61561656 | Common:2; Rare:86 | ||||
| chr3:62318927-62319049 | Rare:49 | ||||
| chr3:63863771-63864157 | Common:8; Rare:128 |