| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37671639-37671745 | Common:1; Rare:51 | ||||
| chr2:37925257-37925406 | Common:3; Rare:64 | ||||
| chr2:38076143-38076265 | Rare:28 | ||||
| chr2:38602871-38603085 | Common:3; Rare:96 | ||||
| chr2:38665844-38666146 | Common:3; Rare:80 | ||||
| chr2:38875815-38876040 | Common:2; Rare:73 | ||||
| chr2:39120373-39120775 | Common:1; Rare:152; Clinvar:2; Clinvar (benign):6 | ||||
| chr2:39120976-39121102 | Common:1; Rare:45 | ||||
| chr2:39436890-39436979 | Rare:27 | ||||
| chr2:39437078-39437464 | Common:4; Rare:138 | ||||
| chr2:42169168-42169492 | Common:1; Rare:153 | ||||
| chr2:42792462-42792766 | Common:2; Rare:104 | ||||
| chr2:43225835-43225946 | Rare:36 | ||||
| chr2:43225958-43226149 | Common:1; Rare:74 | ||||
| chr2:43226216-43226419 | Rare:93 |