| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120710332-120710524 | Common:4; Rare:114 | ||||
| chr12:120725675-120725914 | Common:3; Rare:124; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:120902707-120903350 | Common:9; Rare:135 | ||||
| chr12:120903380-120903690 | Rare:168 | ||||
| chr12:120904077-120904543 | Common:13; Rare:346 | ||||
| chr12:121038973-121039461 | Common:7; Rare:153 | ||||
| chr12:121209884-121210215 | Common:12; Rare:225 | ||||
| chr12:121210163-121210307 | Rare:60 | ||||
| chr12:121210452-121210688 | Common:1; Rare:33 | ||||
| chr12:121296130-121296530 | Rare:79 | ||||
| chr12:121296619-121297048 | Common:6; Rare:315 | ||||
| chr12:121352154-121352687 | Common:10; Rare:409 | ||||
| chr12:121399762-121400215 | Common:15; Rare:445 | ||||
| chr12:121536910-121537428 | Common:7; Rare:186 | ||||
| chr12:121537338-121538227 | Common:8; Rare:501 |