| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56007616-56007902 | Common:2; Rare:73 | ||||
| chr12:56041608-56041978 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr12:56079769-56080248 | Common:4; Rare:110 | ||||
| chr12:56083020-56083432 | Rare:57 | ||||
| chr12:56104198-56104749 | Common:5; Rare:186 | ||||
| chr12:56116309-56116806 | Common:3; Rare:174 | ||||
| chr12:56117982-56118290 | Rare:99 | ||||
| chr12:56127888-56128311 | Rare:85 | ||||
| chr12:56152474-56152624 | Rare:46 | ||||
| chr12:56158211-56158401 | Rare:61 | ||||
| chr12:56189457-56189673 | Rare:77 | ||||
| chr12:56221846-56222030 | Common:1; Rare:48 | ||||
| chr12:56258301-56258532 | Common:1; Rare:79 | ||||
| chr12:56267061-56267310 | Common:2; Rare:65 | ||||
| chr12:56267555-56267654 | Rare:17 |