| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:130871755-130872126 | Common:4; Rare:148 | ||||
| chr12:131710812-131711125 | Rare:81 | ||||
| chr12:131929033-131929286 | Common:10; Rare:77; Clinvar:1 | ||||
| chr12:132687303-132687685 | Common:4; Rare:141; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132828820-132829241 | Common:4; Rare:157 | ||||
| chr12:132887553-132887850 | Rare:86 | ||||
| chr12:132956242-132956447 | Common:1; Rare:43 | ||||
| chr12:132986210-132986434 | Rare:51 | ||||
| chr12:133037220-133037554 | Common:4; Rare:72 | ||||
| chr12:133130238-133130662 | Common:7; Rare:142 | ||||
| chr12:133181369-133181567 | Common:1; Rare:60 | ||||
| chr13:19633365-19633754 | Common:1; Rare:146 | ||||
| chr13:19782923-19783094 | Common:2; Rare:59 | ||||
| chr13:19863441-19863866 | Common:5; Rare:147 | ||||
| chr13:19958458-19958945 | Common:7; Rare:210 |