| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57498264-57498551 | Common:2; Rare:98; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57893827-57894268 | Common:2; Rare:58 | ||||
| chr12:57936026-57936249 | Common:3; Rare:62 | ||||
| chr12:58529915-58530182 | Rare:57 | ||||
| chr12:65447959-65448194 | Rare:27 | ||||
| chr12:65458076-65458088 | Rare:2 | ||||
| chr12:65458284-65458426 | Rare:25 | ||||
| chr12:65467058-65467146 | Common:1; Rare:7 | ||||
| chr12:65499746-65499991 | Common:1; Rare:48 | ||||
| chr12:65545366-65545469 | Rare:18 | ||||
| chr12:65550040-65550190 | Common:1; Rare:29 | ||||
| chr12:65552320-65552371 | Rare:10 | ||||
| chr12:65557452-65557745 | Rare:49 | ||||
| chr12:65561212-65561341 | Rare:23 | ||||
| chr12:65602634-65602887 | Common:1; Rare:37 |