| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50085085-50085399 | Common:1; Rare:84 | ||||
| chr12:50103881-50104053 | Rare:44 | ||||
| chr12:50111960-50112296 | Common:2; Rare:78 | ||||
| chr12:50167307-50167664 | Common:1; Rare:97 | ||||
| chr12:50283452-50283672 | Common:3; Rare:68 | ||||
| chr12:50763957-50764297 | Common:1; Rare:89 | ||||
| chr12:50924459-50924744 | Common:3; Rare:80 | ||||
| chr12:51026313-51026542 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048111-51048364 | Common:2; Rare:86 | ||||
| chr12:51172783-51172915 | Common:2; Rare:30 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270267-51270367 | Common:3; Rare:28 | ||||
| chr12:51270371-51270587 | Common:4; Rare:50 | ||||
| chr12:51887981-51888128 | Rare:36 | ||||
| chr12:52051152-52051470 | Common:1; Rare:105 |