| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27450113-27450220 | Common:3; Rare:33 | ||||
| chr13:27450518-27450643 | Common:2; Rare:54 | ||||
| chr13:28659058-28659184 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr13:30306984-30307197 | Common:5; Rare:50 | ||||
| chr13:30307383-30307615 | Common:3; Rare:76 | ||||
| chr13:30465795-30466128 | Common:1; Rare:105 | ||||
| chr13:30617277-30617392 | Rare:24 | ||||
| chr13:30617579-30618005 | Common:1; Rare:130 | ||||
| chr13:32031518-32031648 | Rare:24 | ||||
| chr13:32315342-32315552 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32586234-32586574 | Common:2; Rare:102 | ||||
| chr13:33206007-33206147 | Rare:29 | ||||
| chr13:33285677-33285861 | Rare:37 | ||||
| chr13:36345553-36345657 | Common:1; Rare:19 | ||||
| chr13:36346301-36346454 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 |