| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50763957-50764166 | Common:1; Rare:56 | ||||
| chr12:51026308-51026496 | Common:3; Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048197-51048379 | Common:1; Rare:81 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51391644-51391732 | Rare:25 | ||||
| chr12:52006690-52006946 | Rare:52 | ||||
| chr12:52043530-52043714 | Common:3; Rare:41 | ||||
| chr12:52051152-52051499 | Common:1; Rare:113 | ||||
| chr12:52948925-52949143 | Common:1; Rare:56 | ||||
| chr12:53006117-53006493 | Common:4; Rare:136 | ||||
| chr12:53046967-53047015 | Common:1; Rare:10 | ||||
| chr12:53047022-53047353 | Common:1; Rare:84 | ||||
| chr12:53048878-53049232 | Common:1; Rare:75 | ||||
| chr12:53049965-53050195 | Common:1; Rare:68 | ||||
| chr12:53054213-53054277 | Rare:16 |