| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97994956-97995291 | Common:4; Rare:131 | ||||
| chr2:97995815-97995931 | Common:1; Rare:40 | ||||
| chr2:97996125-97996389 | Common:2; Rare:90 | ||||
| chr2:98346400-98346510 | Rare:33 | ||||
| chr2:98444732-98444913 | Rare:78 | ||||
| chr2:98608478-98608649 | Common:1; Rare:76 | ||||
| chr2:98608824-98609449 | Common:4; Rare:196 | ||||
| chr2:98731082-98731281 | Common:3; Rare:74 | ||||
| chr2:99141111-99141347 | Common:1; Rare:94 | ||||
| chr2:99141430-99141770 | Common:2; Rare:122 | ||||
| chr2:99154875-99155103 | Common:2; Rare:92; Clinvar (benign):3 | ||||
| chr2:99180971-99181236 | Common:2; Rare:77 | ||||
| chr2:99181323-99181525 | Rare:46 | ||||
| chr2:99336285-99336637 | Common:2; Rare:105 | ||||
| chr2:99337202-99337480 | Rare:96 |