| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219229336-219229419 | Rare:28 | ||||
| chr2:219229582-219229891 | Common:2; Rare:90 | ||||
| chr2:219245416-219245511 | Rare:24 | ||||
| chr2:219279207-219279425 | Common:2; Rare:69 | ||||
| chr2:219498638-219498925 | Common:2; Rare:61 | ||||
| chr2:219597737-219597884 | Common:1; Rare:50 | ||||
| chr2:221572266-221572528 | Common:6; Rare:94 | ||||
| chr2:221573963-221574059 | Rare:22 | ||||
| chr2:223957256-223957468 | Common:4; Rare:78 | ||||
| chr2:226799174-226799282 | Common:1; Rare:27 | ||||
| chr2:226799811-226800141 | Common:1; Rare:93 | ||||
| chr2:226835805-226836100 | Rare:118 | ||||
| chr2:227325191-227325369 | Common:5; Rare:59 | ||||
| chr2:227717985-227718165 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:227871571-227871684 | Common:5; Rare:42 |