| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100670058-100670347 | Rare:59 | ||||
| chr12:101298483-101298647 | Rare:25 | ||||
| chr12:101299588-101299687 | Rare:17 | ||||
| chr12:101299913-101300273 | Common:3; Rare:82 | ||||
| chr12:101749154-101749241 | Rare:23; Clinvar (pathogenic):1 | ||||
| chr12:102481722-102481828 | Common:2; Rare:23 | ||||
| chr12:102742717-102742853 | Rare:25 | ||||
| chr12:103334494-103334744 | Rare:42 | ||||
| chr12:103931237-103931638 | Common:1; Rare:74 | ||||
| chr12:103946615-103946941 | Rare:85 | ||||
| chr12:106193506-106193833 | Rare:51 | ||||
| chr12:108689938-108690169 | Rare:39 | ||||
| chr12:108724427-108724586 | Rare:17 | ||||
| chr12:108727251-108727424 | Common:1; Rare:23 | ||||
| chr12:108802331-108802434 | Rare:14 |