| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120597279-120597304 | Common:1; Rare:3 | ||||
| chr3:120597830-120598060 | Common:2; Rare:32 | ||||
| chr3:120678376-120678531 | Rare:28 | ||||
| chr3:120678640-120678756 | Rare:18 | ||||
| chr3:120688238-120688388 | Rare:25 | ||||
| chr3:120781102-120781393 | Common:3; Rare:82 | ||||
| chr3:121548782-121548965 | Common:1; Rare:31 | ||||
| chr3:121549075-121549122 | Rare:4 | ||||
| chr3:121659439-121659639 | Rare:36 | ||||
| chr3:121809353-121809510 | Rare:22 | ||||
| chr3:121836201-121836334 | Rare:22 | ||||
| chr3:122005103-122005359 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:122058456-122058655 | Rare:45 | ||||
| chr3:122064067-122064149 | Rare:14 | ||||
| chr3:122074750-122074818 | Rare:12 |