| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32755870-32756006 | Rare:48 | ||||
| chr12:34022284-34022522 | Common:2; Rare:63 | ||||
| chr12:40224870-40225063 | Common:4; Rare:50; Clinvar (benign):1 | ||||
| chr12:42325963-42325988 | Rare:6 | ||||
| chr12:42326065-42326226 | Common:1; Rare:52 | ||||
| chr12:42483608-42483746 | Common:1; Rare:33 | ||||
| chr12:42590022-42590163 | Rare:27 | ||||
| chr12:43758720-43759012 | Common:2; Rare:87; Clinvar:2 | ||||
| chr12:45216014-45216158 | Rare:43 | ||||
| chr12:45729559-45729745 | Rare:56 | ||||
| chr12:45990508-45990900 | Common:2; Rare:125 | ||||
| chr12:46268549-46269074 | Common:1; Rare:136 | ||||
| chr12:46364303-46364412 | Common:1; Rare:26 | ||||
| chr12:46367074-46367307 | Common:2; Rare:65 | ||||
| chr12:46370509-46370835 | Rare:76 |