| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42958849-42959077 | Common:2; Rare:61; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:43358690-43358986 | Common:7; Rare:91 | ||||
| chr1:43367934-43368216 | Rare:71 | ||||
| chr1:43389763-43389950 | Common:3; Rare:81 | ||||
| chr1:43946585-43947022 | Rare:122 | ||||
| chr1:43974808-43974972 | Common:3; Rare:48 | ||||
| chr1:44674406-44674749 | Common:3; Rare:92 | ||||
| chr1:44775478-44775615 | Common:1; Rare:55 | ||||
| chr1:44775841-44776140 | Common:2; Rare:108 | ||||
| chr1:44777604-44778074 | Common:2; Rare:115 | ||||
| chr1:44986501-44986825 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:45012034-45012274 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45339996-45340178 | Rare:54 | ||||
| chr1:45340408-45340480 | Common:1; Rare:18; Clinvar:1 | ||||
| chr1:45500046-45500385 | Common:1; Rare:94; Clinvar:5; Clinvar (pathogenic):3 |