| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905431-38905786 | Common:8; Rare:141 | ||||
| chr12:38906067-38906313 | Common:2; Rare:52 | ||||
| chr12:38906640-38907016 | Common:4; Rare:137 | ||||
| chr12:39443087-39443472 | Common:3; Rare:214; Clinvar:14; Clinvar (benign):9 | ||||
| chr12:40105970-40106266 | Common:2; Rare:201 | ||||
| chr12:40224260-40224700 | Common:2; Rare:103 | ||||
| chr12:42144602-42145046 | Common:19; Rare:347 | ||||
| chr12:42237360-42237980 | Common:2; Rare:270 | ||||
| chr12:42238174-42238483 | Common:1; Rare:198 | ||||
| chr12:42326052-42326229 | Common:3; Rare:112 | ||||
| chr12:43758715-43759061 | Common:4; Rare:167; Clinvar:4 | ||||
| chr12:43806305-43806433 | Common:2; Rare:69 | ||||
| chr12:43835470-43836167 | Common:5; Rare:266 | ||||
| chr12:43836220-43836590 | Common:6; Rare:127 | ||||
| chr12:45215961-45216163 | Common:4; Rare:128 |