| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98847927-98848151 | Common:1; Rare:44 | ||||
| chr13:98978346-98978635 | Common:3; Rare:43 | ||||
| chr13:99086611-99086789 | Common:2; Rare:76 | ||||
| chr13:99200668-99200924 | Common:6; Rare:121 | ||||
| chr13:99367785-99368126 | Common:2; Rare:93 | ||||
| chr13:100088921-100089133 | Rare:78; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100641787-100642071 | Common:2; Rare:53 | ||||
| chr13:100674759-100675053 | Common:3; Rare:116 | ||||
| chr13:101452584-101452713 | Common:1; Rare:27 | ||||
| chr13:102596785-102597059 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr13:102597170-102597198 | Rare:5 | ||||
| chr13:102649134-102649487 | Common:4; Rare:73 | ||||
| chr13:102773699-102773843 | Rare:64 | ||||
| chr13:102798921-102799363 | Common:1; Rare:89 | ||||
| chr13:102820389-102820685 | Common:2; Rare:43 |