| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6928277-6928677 | Common:3; Rare:103 | ||||
| chr12:6938060-6938590 | Common:4; Rare:167 | ||||
| chr12:6943528-6943820 | Common:7; Rare:237 | ||||
| chr12:6943926-6944158 | Common:11; Rare:390; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944233-6944428 | Common:1; Rare:71 | ||||
| chr12:6946447-6946645 | Common:1; Rare:47 | ||||
| chr12:6970499-6971074 | Common:18; Rare:328; Clinvar (benign):4 | ||||
| chr12:7018360-7018715 | Common:3; Rare:188 | ||||
| chr12:7018750-7019100 | Common:4; Rare:131 | ||||
| chr12:7060396-7060819 | Rare:161 | ||||
| chr12:7108422-7108734 | Common:2; Rare:168 | ||||
| chr12:7109180-7109280 | Rare:30 | ||||
| chr12:7189498-7189743 | Rare:161; Clinvar:8 | ||||
| chr12:7369210-7369851 | Common:2; Rare:308 | ||||
| chr12:8032589-8032836 | Rare:140 |