| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25878431-25878699 | Common:2; Rare:76 | ||||
| chr2:25982457-25982620 | Common:1; Rare:39 | ||||
| chr2:26033725-26034234 | Common:4; Rare:191 | ||||
| chr2:26034294-26034611 | Common:3; Rare:89 | ||||
| chr2:26244540-26244981 | Common:2; Rare:160; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345789-26346193 | Common:1; Rare:120 | ||||
| chr2:26764191-26764351 | Common:2; Rare:62 | ||||
| chr2:27032862-27033004 | Rare:55 | ||||
| chr2:27071503-27071872 | Common:1; Rare:109 | ||||
| chr2:27211794-27212027 | Common:3; Rare:74 | ||||
| chr2:27212252-27212371 | Common:1; Rare:59 | ||||
| chr2:27217225-27217481 | Rare:102 | ||||
| chr2:27323047-27323141 | Rare:24; Clinvar (benign):1 | ||||
| chr2:27356743-27357087 | Rare:96 | ||||
| chr2:27370247-27370648 | Common:1; Rare:162 |