| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122285428-122285633 | Rare:34 | ||||
| chr12:122327944-122328426 | Common:5; Rare:149 | ||||
| chr12:122352730-122352987 | Rare:61 | ||||
| chr12:122400554-122400725 | Rare:24 | ||||
| chr12:122521384-122521507 | Rare:36 | ||||
| chr12:122721165-122721411 | Rare:52 | ||||
| chr12:122753520-122753806 | Rare:78 | ||||
| chr12:122763429-122763748 | Common:2; Rare:71 | ||||
| chr12:122863976-122864112 | Common:2; Rare:22 | ||||
| chr12:123150997-123151157 | Common:2; Rare:43 | ||||
| chr12:123327746-123327970 | Rare:47 | ||||
| chr12:123630208-123630489 | Rare:62; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:124918397-124918686 | Common:1; Rare:54 | ||||
| chr12:124923528-124923657 | Common:1; Rare:27 | ||||
| chr12:124928713-124928786 | Rare:13 |