| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124354559-124354848 | Common:3; Rare:83 | ||||
| chr12:124390744-124390938 | Common:1; Rare:44 | ||||
| chr12:127060315-127060618 | Common:4; Rare:99 | ||||
| chr12:127146001-127146181 | Rare:61 | ||||
| chr12:128844254-128844278 | Rare:3 | ||||
| chr12:128852422-128852713 | Common:1; Rare:58 | ||||
| chr12:128854333-128854604 | Common:2; Rare:45 | ||||
| chr12:128857394-128857615 | Common:1; Rare:41 | ||||
| chr12:131896149-131896230 | Rare:22 | ||||
| chr12:131897062-131897164 | Common:1; Rare:14 | ||||
| chr12:132104664-132104929 | Common:4; Rare:86 | ||||
| chr12:132189672-132189994 | Common:7; Rare:113 | ||||
| chr12:132664116-132664368 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):5 | ||||
| chr13:19344821-19344958 | Common:1; Rare:26 | ||||
| chr13:19649864-19650038 | Common:2; Rare:32 |