| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24793018-24793171 | Rare:66 | ||||
| chr2:24971913-24972145 | Common:1; Rare:73 | ||||
| chr2:26033753-26034159 | Common:4; Rare:153 | ||||
| chr2:26244563-26244972 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346165 | Common:1; Rare:110 | ||||
| chr2:27032841-27033000 | Rare:62 | ||||
| chr2:27211920-27212088 | Common:3; Rare:64 | ||||
| chr2:27212242-27212376 | Common:1; Rare:68 | ||||
| chr2:27217267-27217405 | Rare:56 | ||||
| chr2:27323029-27323154 | Rare:34; Clinvar (benign):1 | ||||
| chr2:27356750-27357071 | Rare:92 | ||||
| chr2:27370259-27370641 | Common:1; Rare:158 | ||||
| chr2:27628973-27629122 | Common:1; Rare:84 | ||||
| chr2:27663369-27663469 | Rare:28 | ||||
| chr2:27663545-27663947 | Rare:155 |