| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45727586-45727890 | Common:2; Rare:98 | ||||
| chr12:46383313-46383712 | Common:3; Rare:123 | ||||
| chr12:46383903-46384026 | Rare:36 | ||||
| chr12:46524281-46524455 | Common:1; Rare:25 | ||||
| chr12:46652409-46652430 | |||||
| chr12:46793055-46793312 | Rare:43 | ||||
| chr12:46917110-46917152 | Rare:11 | ||||
| chr12:46983979-46984282 | Rare:54 | ||||
| chr12:48688269-48688525 | Common:1; Rare:40 | ||||
| chr12:49005003-49005157 | Common:1; Rare:30 | ||||
| chr12:49185970-49186019 | Rare:12; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:49494065-49494410 | Common:1; Rare:53 | ||||
| chr12:52057491-52057633 | Rare:43 | ||||
| chr12:53100710-53101111 | Common:3; Rare:133 | ||||
| chr12:53221555-53221795 | Common:4; Rare:52 |