| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69179914-69180315 | Common:3; Rare:131 | ||||
| chr10:69451297-69451612 | Common:2; Rare:86 | ||||
| chr10:70052475-70052926 | Common:1; Rare:95 | ||||
| chr10:70132729-70132955 | Common:2; Rare:62 | ||||
| chr10:70163507-70163803 | Common:4; Rare:57 | ||||
| chr10:70170414-70170722 | Common:4; Rare:98 | ||||
| chr10:70233281-70233535 | Common:6; Rare:95; Clinvar (benign):1 | ||||
| chr10:70404343-70404543 | Common:1; Rare:64 | ||||
| chr10:70478538-70478819 | Rare:91 | ||||
| chr10:70815884-70816123 | Rare:83 | ||||
| chr10:70816458-70816727 | Rare:49 | ||||
| chr10:70888229-70888383 | Common:2; Rare:36 | ||||
| chr10:70888532-70888679 | Common:2; Rare:45; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:71773450-71773666 | Common:3; Rare:72 | ||||
| chr10:71819140-71819253 | Rare:26 |