| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018744-49019029 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr12:49131331-49131603 | Common:2; Rare:109 | ||||
| chr12:49568110-49568192 | Common:2; Rare:28 | ||||
| chr12:49828407-49828703 | Rare:83 | ||||
| chr12:50924557-50924705 | Common:1; Rare:30 | ||||
| chr12:52948931-52949159 | Common:1; Rare:63 | ||||
| chr12:52949822-52950030 | Rare:45 | ||||
| chr12:53097367-53097673 | Rare:56 | ||||
| chr12:53097733-53098224 | Common:2; Rare:131 | ||||
| chr12:53299436-53299710 | Common:2; Rare:76 | ||||
| chr12:55716020-55716083 | Common:1; Rare:30 | ||||
| chr12:55725843-55726259 | Rare:95 | ||||
| chr12:55726890-55727229 | Common:2; Rare:110 | ||||
| chr12:55728321-55728482 | Rare:50 | ||||
| chr12:55728912-55729127 | Common:1; Rare:39 |