| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:69348251-69348553 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:69470283-69470439 | Common:3; Rare:61 | ||||
| chr12:70242884-70243039 | Common:1; Rare:55 | ||||
| chr12:71663346-71663613 | Rare:117 | ||||
| chr12:71663763-71664042 | Common:1; Rare:82 | ||||
| chr12:71664284-71664477 | Rare:55 | ||||
| chr12:71686018-71686120 | Common:1; Rare:28 | ||||
| chr12:71686432-71686531 | Common:1; Rare:26 | ||||
| chr12:71839515-71839806 | Common:3; Rare:96 | ||||
| chr12:72272277-72272563 | Common:3; Rare:61 | ||||
| chr12:74537770-74537889 | Common:1; Rare:50 | ||||
| chr12:74538252-74538314 | Rare:18 | ||||
| chr12:75390876-75391142 | Common:1; Rare:89 | ||||
| chr12:75480659-75480904 | Rare:54 | ||||
| chr12:75511573-75511674 | Rare:43 |