| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56315219-56315485 | Rare:70 | ||||
| chr12:56315828-56316101 | Common:1; Rare:68 | ||||
| chr12:56333936-56334113 | Rare:48 | ||||
| chr12:56468478-56468583 | Rare:47 | ||||
| chr12:56636208-56636456 | Common:1; Rare:47 | ||||
| chr12:56644921-56645362 | Common:1; Rare:102 | ||||
| chr12:56645835-56645928 | Rare:39 | ||||
| chr12:57039061-57039283 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr12:57039399-57039542 | Rare:19 | ||||
| chr12:57096964-57097122 | Rare:53 | ||||
| chr12:57111173-57111436 | Common:4; Rare:51 | ||||
| chr12:57111802-57111903 | Common:1; Rare:19 | ||||
| chr12:57128348-57128769 | Common:1; Rare:79 | ||||
| chr12:57201496-57201799 | Common:2; Rare:72 | ||||
| chr12:57202216-57202535 | Common:2; Rare:75 |