| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93677776-93678037 | Common:1; Rare:46 | ||||
| chr12:93678084-93678333 | Rare:36 | ||||
| chr12:94262292-94262738 | Common:2; Rare:98 | ||||
| chr12:94262941-94263095 | Common:1; Rare:36 | ||||
| chr12:94458975-94459220 | Rare:45 | ||||
| chr12:94459325-94459420 | Common:1; Rare:16 | ||||
| chr12:94459523-94460136 | Common:8; Rare:165 | ||||
| chr12:94460424-94460515 | Rare:22 | ||||
| chr12:94615290-94615688 | Common:2; Rare:69 | ||||
| chr12:94615961-94616088 | Rare:24 | ||||
| chr12:94649990-94650112 | Rare:31 | ||||
| chr12:94650442-94650613 | Common:2; Rare:57 | ||||
| chr12:95003210-95003432 | Common:1; Rare:43 | ||||
| chr12:95003582-95003841 | Common:3; Rare:111; Clinvar (benign):6 | ||||
| chr12:95072868-95073129 | Common:2; Rare:79 |