| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26244581-26244943 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345798-26346165 | Common:1; Rare:110 | ||||
| chr2:26764188-26764298 | Common:1; Rare:38 | ||||
| chr2:26785768-26786032 | Rare:64 | ||||
| chr2:27032848-27032995 | Rare:58 | ||||
| chr2:27051546-27051696 | Rare:43 | ||||
| chr2:27071609-27071888 | Common:1; Rare:85 | ||||
| chr2:27086535-27086759 | Common:3; Rare:69 | ||||
| chr2:27211794-27212065 | Common:3; Rare:93 | ||||
| chr2:27212252-27212379 | Common:1; Rare:64 | ||||
| chr2:27217222-27217530 | Rare:120 | ||||
| chr2:27263038-27263192 | Rare:37 | ||||
| chr2:27323043-27323154 | Rare:27; Clinvar (benign):1 | ||||
| chr2:27356437-27356561 | Rare:52 | ||||
| chr2:27356743-27357087 | Rare:96 |