| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:72335521-72335624 | Rare:27 | ||||
| chr10:72566670-72567070 | Rare:86; Clinvar (pathogenic):1 | ||||
| chr10:73067180-73067858 | Common:6; Rare:153 | ||||
| chr10:73076877-73077277 | Common:4; Rare:91 | ||||
| chr10:73079750-73080070 | Rare:92 | ||||
| chr10:73094341-73094816 | Common:3; Rare:122 | ||||
| chr10:73095439-73095654 | Common:1; Rare:43 | ||||
| chr10:73095598-73095724 | Common:1; Rare:21 | ||||
| chr10:73096084-73096334 | Common:2; Rare:115 | ||||
| chr10:73118064-73118294 | Rare:70 | ||||
| chr10:73246744-73247080 | Common:4; Rare:389 | ||||
| chr10:73247030-73247480 | Common:1; Rare:614 | ||||
| chr10:73398220-73398510 | Rare:68 | ||||
| chr10:73413118-73413440 | Common:4; Rare:70 | ||||
| chr10:73414783-73415028 | Common:1; Rare:43 |