| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50103882-50104051 | Rare:42 | ||||
| chr12:50111941-50112276 | Common:2; Rare:79 | ||||
| chr12:50283424-50283665 | Common:2; Rare:71 | ||||
| chr12:50763931-50764331 | Common:1; Rare:107 | ||||
| chr12:50924426-50924755 | Common:3; Rare:88 | ||||
| chr12:51026313-51026542 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048117-51048359 | Common:1; Rare:82 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270278-51270306 | Rare:7 | ||||
| chr12:51270375-51270480 | Rare:28 | ||||
| chr12:51391402-51391464 | Rare:14 | ||||
| chr12:51391613-51391736 | Common:1; Rare:39 | ||||
| chr12:51590740-51590933 | Common:1; Rare:58 | ||||
| chr12:52948812-52949214 | Common:2; Rare:108; Clinvar:1 | ||||
| chr12:52949822-52950136 | Rare:62 |