| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633583-123633868 | Common:2; Rare:141; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123671349-123671532 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr12:123712288-123712577 | Common:4; Rare:103; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:123723196-123723318 | Rare:27 | ||||
| chr12:123762067-123762348 | Common:1; Rare:79 | ||||
| chr12:123944260-123944522 | Rare:56 | ||||
| chr12:123972558-123972895 | Common:6; Rare:117 | ||||
| chr12:123973008-123973328 | Common:2; Rare:107 | ||||
| chr12:123997569-123997713 | Common:1; Rare:21 | ||||
| chr12:124388791-124388978 | Common:3; Rare:57 | ||||
| chr12:124786428-124786793 | Common:3; Rare:97 | ||||
| chr12:124913998-124914199 | Common:7; Rare:78 | ||||
| chr12:124914567-124915097 | Common:9; Rare:215 | ||||
| chr12:124915262-124915517 | Common:2; Rare:64 | ||||
| chr12:124917332-124917424 | Rare:30 |