| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25878089-25878242 | Rare:47 | ||||
| chr2:25878346-25878850 | Common:5; Rare:144 | ||||
| chr2:26033520-26033652 | Rare:31 | ||||
| chr2:26033661-26034288 | Common:5; Rare:217 | ||||
| chr2:26034380-26034465 | Rare:17 | ||||
| chr2:26184762-26184968 | Rare:44 | ||||
| chr2:26244278-26244427 | Rare:28 | ||||
| chr2:26244527-26245046 | Common:2; Rare:176; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:26345710-26346227 | Common:2; Rare:156 | ||||
| chr2:26346718-26346899 | Rare:30 | ||||
| chr2:26764156-26764362 | Common:2; Rare:84 | ||||
| chr2:26785653-26786167 | Common:1; Rare:129 | ||||
| chr2:27032559-27033043 | Common:1; Rare:126 | ||||
| chr2:27050358-27050839 | Common:4; Rare:177 | ||||
| chr2:27051012-27051213 | Common:4; Rare:81 |