| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51391397-51391458 | Common:1; Rare:12 | ||||
| chr12:51391592-51391736 | Common:1; Rare:43 | ||||
| chr12:52051110-52051493 | Common:1; Rare:128 | ||||
| chr12:52055857-52056149 | Common:3; Rare:89 | ||||
| chr12:52070168-52070259 | Rare:27 | ||||
| chr12:52492622-52492997 | Common:5; Rare:127; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr12:52949784-52950030 | Rare:55 | ||||
| chr12:52951476-52951856 | Rare:102; Clinvar:5 | ||||
| chr12:53006096-53006495 | Common:4; Rare:148 | ||||
| chr12:53048855-53049221 | Common:1; Rare:76 | ||||
| chr12:53054425-53054579 | Common:2; Rare:53 | ||||
| chr12:53079333-53079594 | Common:2; Rare:88 | ||||
| chr12:53097325-53097682 | Common:1; Rare:72 | ||||
| chr12:53180494-53180583 | Common:1; Rare:34 | ||||
| chr12:53180599-53180700 | Rare:35 |