| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120252527-120252981 | Common:3; Rare:140 | ||||
| chr2:120253131-120253340 | Common:1; Rare:57 | ||||
| chr2:120253750-120253886 | Rare:24 | ||||
| chr2:121530237-121530447 | Rare:58 | ||||
| chr2:121530539-121531308 | Common:19; Rare:562; Clinvar (pathogenic):15 | ||||
| chr2:121648830-121649180 | Common:3; Rare:79 | ||||
| chr2:121649390-121649860 | Common:2; Rare:133 | ||||
| chr2:121649919-121650175 | Common:1; Rare:69 | ||||
| chr2:121736724-121737309 | Common:5; Rare:235 | ||||
| chr2:121755381-121755875 | Common:6; Rare:160 | ||||
| chr2:126655780-126656484 | Common:1; Rare:213; Clinvar:2 | ||||
| chr2:126656567-126656747 | Rare:41 | ||||
| chr2:127064873-127065115 | Rare:56 | ||||
| chr2:127107026-127107377 | Common:4; Rare:107; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:127294047-127294277 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):2 |