| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128765214-128765281 | Rare:6 | ||||
| chr3:128777873-128778004 | Common:2; Rare:21 | ||||
| chr3:128798864-128799021 | Common:1; Rare:22 | ||||
| chr3:128807541-128807858 | Rare:68; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr3:128906565-128906818 | Common:1; Rare:48 | ||||
| chr3:129120619-129120841 | Common:1; Rare:48 | ||||
| chr3:129155438-129155714 | Common:1; Rare:51 | ||||
| chr3:129250456-129250733 | Common:1; Rare:74 | ||||
| chr3:129252348-129252989 | Common:1; Rare:159 | ||||
| chr3:129257573-129257858 | Common:2; Rare:103 | ||||
| chr3:129258961-129258990 | Rare:5 | ||||
| chr3:129262911-129263326 | Common:10; Rare:86 | ||||
| chr3:129273441-129273466 | Rare:5 | ||||
| chr3:129279585-129279847 | Rare:68 | ||||
| chr3:129281715-129281775 | Rare:9 |