| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98533812-98533961 | Common:1; Rare:42; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:98592904-98593040 | Rare:25 | ||||
| chr12:98644079-98644229 | Rare:25 | ||||
| chr12:98644233-98644335 | Rare:16 | ||||
| chr12:98814314-98814557 | Rare:36 | ||||
| chr12:98916006-98916415 | Common:1; Rare:73 | ||||
| chr12:98973479-98973658 | Common:2; Rare:22 | ||||
| chr12:99059968-99060033 | Common:1; Rare:8 | ||||
| chr12:99131168-99131329 | Rare:27 | ||||
| chr12:99131641-99131839 | Rare:44 | ||||
| chr12:99131949-99132150 | Common:1; Rare:34 | ||||
| chr12:99238283-99238528 | Common:1; Rare:53 | ||||
| chr12:100142179-100142306 | Common:2; Rare:31 | ||||
| chr12:100163967-100164157 | Common:1; Rare:59 | ||||
| chr12:100574428-100574445 | Rare:3 |