| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111597101-111597463 | Rare:67 | ||||
| chr12:111597952-111598039 | Rare:31 | ||||
| chr12:111598523-111598593 | Rare:18 | ||||
| chr12:111599062-111599138 | Common:2; Rare:24; Clinvar (benign):1 | ||||
| chr12:111599257-111599490 | Common:2; Rare:83 | ||||
| chr12:111599553-111600044 | Common:2; Rare:139 | ||||
| chr12:111685875-111686196 | Rare:112 | ||||
| chr12:111766795-111766995 | Rare:64 | ||||
| chr12:111841442-111841587 | Rare:31 | ||||
| chr12:111841829-111842589 | Common:7; Rare:197 | ||||
| chr12:111842638-111842867 | Rare:72 | ||||
| chr12:112006040-112006159 | Common:4; Rare:14 | ||||
| chr12:112012675-112012856 | Rare:31 | ||||
| chr12:112012962-112013543 | Common:1; Rare:195 | ||||
| chr12:112108477-112108839 | Common:2; Rare:99 |