| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194243-106194568 | Common:6; Rare:138 | ||||
| chr2:108288745-108289049 | Common:2; Rare:52 | ||||
| chr2:108449098-108449277 | Rare:73 | ||||
| chr2:108534138-108534502 | Common:7; Rare:148 | ||||
| chr2:108654748-108655058 | Rare:65 | ||||
| chr2:108719372-108719553 | Common:2; Rare:74 | ||||
| chr2:109613833-109614007 | Common:2; Rare:64 | ||||
| chr2:110204941-110205176 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110677997-110678225 | Rare:73 | ||||
| chr2:111122431-111122723 | Common:3; Rare:125 | ||||
| chr2:111884128-111884266 | Rare:40 | ||||
| chr2:111898300-111898618 | Common:2; Rare:70 | ||||
| chr2:112254977-112255197 | Common:2; Rare:92 | ||||
| chr2:112275384-112275642 | Common:1; Rare:91 | ||||
| chr2:112542119-112542490 | Common:1; Rare:116 |