| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:234606251-234606330 | Rare:14 | ||||
| chr1:234606341-234606703 | Common:2; Rare:106 | ||||
| chr1:234607281-234607539 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr1:234610541-234610952 | Common:2; Rare:125 | ||||
| chr1:234610955-234611615 | Common:7; Rare:223 | ||||
| chr1:234611677-234611768 | Rare:18 | ||||
| chr1:234611792-234612274 | Common:3; Rare:98 | ||||
| chr1:234612470-234613119 | Common:2; Rare:93 | ||||
| chr1:234613314-234613404 | Rare:22 | ||||
| chr1:234613432-234613472 | Rare:6 | ||||
| chr1:234613551-234613804 | Rare:35 | ||||
| chr1:234618573-234618604 | Rare:4 | ||||
| chr1:234618797-234618942 | Common:1; Rare:23 | ||||
| chr1:234647845-234647886 | Rare:6 | ||||
| chr1:234656569-234656661 | Common:1; Rare:20 |