| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76878991-76879216 | Rare:76 | ||||
| chr12:77065530-77065770 | Rare:77 | ||||
| chr12:79934910-79935391 | Common:1; Rare:185 | ||||
| chr12:80937676-80937817 | Common:1; Rare:44 | ||||
| chr12:82358232-82358546 | Common:2; Rare:154 | ||||
| chr12:82358742-82358906 | Common:3; Rare:81 | ||||
| chr12:88141878-88142375 | Common:1; Rare:127; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:88580311-88580578 | Common:2; Rare:83 | ||||
| chr12:89352251-89352519 | Common:1; Rare:76 | ||||
| chr12:89524751-89524896 | Common:1; Rare:27 | ||||
| chr12:89525967-89526363 | Rare:111 | ||||
| chr12:89708779-89708969 | Rare:76 | ||||
| chr12:91180494-91180802 | Rare:50 | ||||
| chr12:91182587-91182950 | Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:93377727-93377929 | Rare:54 |