| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68956103-68956309 | Common:2; Rare:79 | ||||
| chr10:69179914-69180354 | Common:3; Rare:150 | ||||
| chr10:69451335-69451616 | Common:2; Rare:78 | ||||
| chr10:69630111-69630316 | Common:1; Rare:63 | ||||
| chr10:69801730-69801987 | Common:1; Rare:66 | ||||
| chr10:70146512-70146891 | Common:1; Rare:102 | ||||
| chr10:70170414-70170694 | Common:4; Rare:92 | ||||
| chr10:70233281-70233625 | Common:6; Rare:121; Clinvar (benign):1 | ||||
| chr10:70403967-70404191 | Rare:82 | ||||
| chr10:70478494-70478839 | Rare:108 | ||||
| chr10:70888180-70888383 | Common:3; Rare:43 | ||||
| chr10:70888531-70888811 | Common:2; Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:71319218-71319304 | Common:2; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71396788-71396965 | Common:2; Rare:36 | ||||
| chr10:71719793-71720121 | Rare:75 |