| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36481604-36481729 | Common:2; Rare:32 | ||||
| chr22:37560327-37560566 | Common:1; Rare:81 | ||||
| chr22:37608679-37608872 | Common:1; Rare:55 | ||||
| chr22:37676689-37677063 | Rare:116 | ||||
| chr22:37849331-37849478 | Rare:81 | ||||
| chr22:38181804-38181925 | Common:1; Rare:33 | ||||
| chr22:38201775-38202094 | Common:2; Rare:92 | ||||
| chr22:38656391-38656678 | Common:1; Rare:63 | ||||
| chr22:38681821-38682026 | Common:2; Rare:87 | ||||
| chr22:38739790-38740099 | Rare:79; Clinvar (benign):1 | ||||
| chr22:39319499-39319797 | Common:5; Rare:138 | ||||
| chr22:39532672-39533037 | Common:2; Rare:143 | ||||
| chr22:40044115-40044341 | Common:2; Rare:52 | ||||
| chr22:40044528-40044862 | Common:2; Rare:78 | ||||
| chr22:40346418-40346585 | Rare:79; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 |