| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194186-106194543 | Common:6; Rare:151 | ||||
| chr2:106887028-106887127 | Common:2; Rare:31 | ||||
| chr2:108288740-108289070 | Common:2; Rare:54 | ||||
| chr2:108378029-108378171 | Common:1; Rare:24 | ||||
| chr2:108449098-108449278 | Rare:74 | ||||
| chr2:108534140-108534528 | Common:7; Rare:157 | ||||
| chr2:108621175-108621287 | Rare:19 | ||||
| chr2:108654659-108655055 | Common:2; Rare:77 | ||||
| chr2:108719395-108719757 | Common:4; Rare:153; Clinvar (benign):3 | ||||
| chr2:109613829-109614003 | Common:2; Rare:63 | ||||
| chr2:110115796-110115945 | Common:2; Rare:36 | ||||
| chr2:110204900-110205109 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:110678032-110678244 | Rare:62 | ||||
| chr2:111122425-111122810 | Common:3; Rare:154 | ||||
| chr2:111884123-111884255 | Rare:39 |