| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44213315-44213548 | Common:1; Rare:51 | ||||
| chr1:44354895-44355005 | Rare:44 | ||||
| chr1:44404980-44405266 | Rare:61 | ||||
| chr1:44405274-44405437 | Common:1; Rare:60 | ||||
| chr1:44631902-44632318 | Common:4; Rare:165 | ||||
| chr1:44674413-44674755 | Common:3; Rare:92 | ||||
| chr1:44739641-44739938 | Common:3; Rare:122 | ||||
| chr1:44760476-44760702 | Rare:58 | ||||
| chr1:44775377-44775615 | Common:2; Rare:95 | ||||
| chr1:44775660-44775871 | Common:2; Rare:68 | ||||
| chr1:44800141-44800379 | Common:1; Rare:54 | ||||
| chr1:44843251-44843513 | Rare:68 | ||||
| chr1:44986527-44986838 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr1:45326748-45327043 | Rare:69 | ||||
| chr1:45339944-45340259 | Common:1; Rare:118; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):1 |