| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21176430-21176978 | Common:6; Rare:230 | ||||
| chr13:21177083-21177161 | Rare:29 | ||||
| chr13:21459227-21459545 | Common:2; Rare:114 | ||||
| chr13:21603675-21604000 | Rare:142 | ||||
| chr13:21604080-21604398 | Common:6; Rare:139 | ||||
| chr13:21670928-21671189 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:21673831-21674204 | Rare:84 | ||||
| chr13:23375300-23375843 | Common:6; Rare:185 | ||||
| chr13:23579156-23579410 | Common:5; Rare:88 | ||||
| chr13:23888720-23888961 | Common:1; Rare:60 | ||||
| chr13:23889303-23889646 | Common:1; Rare:108 | ||||
| chr13:23979667-23979699 | Rare:6 | ||||
| chr13:24160549-24160818 | Common:1; Rare:73 | ||||
| chr13:24270501-24270820 | Common:3; Rare:61 | ||||
| chr13:24270907-24271149 | Common:3; Rare:59 |