| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7089286-7089738 | Common:3; Rare:146 | ||||
| chr12:7124715-7125018 | Rare:62 | ||||
| chr12:7493006-7493309 | Common:1; Rare:44 | ||||
| chr12:7495379-7495545 | Common:1; Rare:35 | ||||
| chr12:7498773-7498779 | |||||
| chr12:9076521-9076562 | Common:1; Rare:7 | ||||
| chr12:9077305-9077477 | Common:1; Rare:47 | ||||
| chr12:9083169-9083229 | Rare:10 | ||||
| chr12:9093438-9093697 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr12:9109311-9109501 | Rare:48 | ||||
| chr12:9110152-9110191 | Rare:5 | ||||
| chr12:9112142-9112234 | Rare:30 | ||||
| chr12:9113604-9113911 | Common:1; Rare:37 | ||||
| chr12:9124649-9124993 | Common:1; Rare:55 | ||||
| chr12:9127419-9127741 | Common:1; Rare:59 |