| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121649381-121649878 | Common:3; Rare:138 | ||||
| chr2:121649938-121650151 | Rare:60 | ||||
| chr2:121736737-121737309 | Common:5; Rare:230 | ||||
| chr2:121755406-121755804 | Common:5; Rare:133 | ||||
| chr2:121755860-121755990 | Rare:39 | ||||
| chr2:127106914-127107297 | Common:1; Rare:117; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:127107334-127107667 | Common:8; Rare:71 | ||||
| chr2:127107839-127107883 | Rare:6 | ||||
| chr2:127293913-127293931 | Rare:7 | ||||
| chr2:127294086-127294266 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387247-127387614 | Common:5; Rare:127 | ||||
| chr2:127387631-127387672 | Rare:10 | ||||
| chr2:127387699-127387797 | Common:1; Rare:25 | ||||
| chr2:127387848-127388381 | Common:10; Rare:206 | ||||
| chr2:127423132-127423352 | Common:2; Rare:72; Clinvar (benign):3; Clinvar (pathogenic):1 |