| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:24494989-24495263 | Common:2; Rare:104; Clinvar:13; Clinvar (benign):10 | ||||
| chr6:24522620-24522925 | Rare:76; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:24666730-24667218 | Common:4; Rare:201 | ||||
| chr6:24720234-24720401 | Common:2; Rare:59 | ||||
| chr6:25279161-25279605 | Common:2; Rare:157 | ||||
| chr6:26033599-26033797 | Common:3; Rare:54 | ||||
| chr6:26043685-26043954 | Common:3; Rare:104 | ||||
| chr6:26055965-26056244 | Common:4; Rare:213 | ||||
| chr6:26056246-26056526 | Common:6; Rare:211 | ||||
| chr6:26103773-26103952 | Common:3; Rare:78 | ||||
| chr6:26123643-26124430 | Common:7; Rare:388 | ||||
| chr6:26124450-26124514 | Rare:21 | ||||
| chr6:26124645-26124710 | Rare:30 | ||||
| chr6:26156303-26156964 | Common:6; Rare:516 | ||||
| chr6:26157876-26158248 | Common:5; Rare:162 |