| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38602048-38602251 | Common:2; Rare:84 | ||||
| chr2:38602828-38603196 | Common:4; Rare:146 | ||||
| chr2:38751342-38751468 | Rare:65 | ||||
| chr2:38778111-38778235 | Rare:28 | ||||
| chr2:38875852-38876026 | Common:2; Rare:57 | ||||
| chr2:39119724-39120455 | Common:5; Rare:387; Clinvar:2; Clinvar (benign):9 | ||||
| chr2:39120992-39121150 | Rare:62 | ||||
| chr2:39121320-39121937 | Common:2; Rare:165 | ||||
| chr2:39124194-39124631 | Common:1; Rare:139 | ||||
| chr2:39436478-39436886 | Common:6; Rare:190 | ||||
| chr2:39437210-39437476 | Common:3; Rare:97 | ||||
| chr2:39665685-39666085 | Common:2; Rare:171 | ||||
| chr2:40451289-40452329 | Common:12; Rare:409 | ||||
| chr2:42047812-42048080 | Common:4; Rare:92 | ||||
| chr2:42169124-42169408 | Common:1; Rare:136 |