| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69123421-69123514 | Common:1; Rare:21 | ||||
| chr10:69179912-69180363 | Common:3; Rare:154 | ||||
| chr10:69269882-69270082 | Common:1; Rare:33 | ||||
| chr10:69451305-69451579 | Common:2; Rare:77 | ||||
| chr10:69494736-69494964 | Common:1; Rare:51 | ||||
| chr10:69494966-69495163 | Common:3; Rare:35 | ||||
| chr10:69630133-69630306 | Common:1; Rare:53 | ||||
| chr10:70052556-70052978 | Rare:93 | ||||
| chr10:70132625-70132920 | Rare:86 | ||||
| chr10:70146604-70146830 | Common:1; Rare:65 | ||||
| chr10:70170448-70170736 | Common:3; Rare:90 | ||||
| chr10:70233319-70233550 | Common:6; Rare:85; Clinvar (benign):1 | ||||
| chr10:70382591-70382849 | Common:4; Rare:94 | ||||
| chr10:70404013-70404200 | Rare:71 | ||||
| chr10:70447964-70448105 | Common:2; Rare:21 |