| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251235-27251632 | Common:8; Rare:123 | ||||
| chr13:27450136-27450223 | Common:3; Rare:26 | ||||
| chr13:27450510-27450651 | Common:2; Rare:58 | ||||
| chr13:28659004-28659178 | Rare:87; Clinvar (pathogenic):1 | ||||
| chr13:30306836-30307211 | Common:6; Rare:104 | ||||
| chr13:30465795-30466134 | Common:1; Rare:107 | ||||
| chr13:30617242-30617375 | Rare:25 | ||||
| chr13:30617579-30617970 | Common:1; Rare:122 | ||||
| chr13:32031230-32031352 | Common:1; Rare:36 | ||||
| chr13:32031726-32031790 | Rare:32 | ||||
| chr13:32315437-32315547 | Rare:35; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32538650-32538933 | Common:1; Rare:79 | ||||
| chr13:33818017-33818238 | Common:1; Rare:101 | ||||
| chr13:36297819-36297908 | Rare:34 | ||||
| chr13:37000500-37000815 | Common:3; Rare:99; Clinvar (pathogenic):1 |