| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57110384-57110393 | Rare:1 | ||||
| chr12:57111173-57111436 | Common:4; Rare:51 | ||||
| chr12:57111803-57111907 | Common:1; Rare:19 | ||||
| chr12:57128307-57128803 | Common:1; Rare:99 | ||||
| chr12:57128921-57129021 | Rare:23 | ||||
| chr12:57201495-57201866 | Common:2; Rare:89 | ||||
| chr12:57230007-57230167 | Rare:33 | ||||
| chr12:57430747-57431057 | Common:1; Rare:74 | ||||
| chr12:57475530-57476035 | Common:5; Rare:159 | ||||
| chr12:57477621-57478130 | Common:2; Rare:148 | ||||
| chr12:57478706-57478962 | Common:1; Rare:54 | ||||
| chr12:57479560-57479706 | Rare:22 | ||||
| chr12:57479836-57479904 | Rare:10 | ||||
| chr12:57488769-57489048 | Common:3; Rare:56; Clinvar (benign):1 | ||||
| chr12:57520494-57520727 | Common:1; Rare:70 |