| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119759752-119760122 | Common:3; Rare:97 | ||||
| chr2:120012954-120013097 | Common:1; Rare:64 | ||||
| chr2:120252626-120252968 | Common:3; Rare:114 | ||||
| chr2:120735592-120735893 | Common:13; Rare:99 | ||||
| chr2:121530340-121530413 | Rare:22 | ||||
| chr2:121530564-121530884 | Common:7; Rare:133 | ||||
| chr2:121649429-121649766 | Common:2; Rare:104 | ||||
| chr2:121649928-121650157 | Rare:63 | ||||
| chr2:121736843-121737105 | Common:4; Rare:94 | ||||
| chr2:121755433-121755848 | Common:5; Rare:133 | ||||
| chr2:127107022-127107358 | Common:4; Rare:105; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:127294100-127294243 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr2:127387459-127387472 | Rare:3 | ||||
| chr2:127387941-127388268 | Common:8; Rare:141 | ||||
| chr2:127526429-127526619 | Common:2; Rare:61 |