| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68721461-68721539 | Rare:25 | ||||
| chr10:68900950-68901386 | Common:3; Rare:170 | ||||
| chr10:68988621-68988830 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chr10:68989040-68989193 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr10:69179918-69180327 | Common:3; Rare:133 | ||||
| chr10:69318626-69318968 | Common:4; Rare:98 | ||||
| chr10:69801646-69801926 | Common:2; Rare:73 | ||||
| chr10:70146647-70146930 | Common:1; Rare:68 | ||||
| chr10:70170454-70170683 | Common:3; Rare:77 | ||||
| chr10:70233310-70233562 | Common:6; Rare:92; Clinvar (benign):1 | ||||
| chr10:70404393-70404451 | Rare:17 | ||||
| chr10:71319171-71319291 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71851204-71851464 | Common:5; Rare:110; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:72273694-72273953 | Rare:72 | ||||
| chr10:72354881-72355196 | Common:2; Rare:112 |