| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69451310-69451524 | Common:2; Rare:55 | ||||
| chr10:69801670-69801914 | Common:2; Rare:64 | ||||
| chr10:70052063-70052381 | Rare:50 | ||||
| chr10:70052456-70052523 | Rare:14 | ||||
| chr10:70052526-70053083 | Common:1; Rare:119 | ||||
| chr10:70053092-70053380 | Common:2; Rare:56 | ||||
| chr10:70145964-70146216 | Common:1; Rare:85 | ||||
| chr10:70146557-70147012 | Common:2; Rare:111 | ||||
| chr10:70170382-70170859 | Common:4; Rare:131 | ||||
| chr10:70233262-70233703 | Common:6; Rare:138; Clinvar (benign):1 | ||||
| chr10:70233892-70234194 | Common:3; Rare:52 | ||||
| chr10:70381841-70381948 | Rare:27 | ||||
| chr10:70381984-70382118 | Rare:27 | ||||
| chr10:70382140-70382168 | Rare:9 | ||||
| chr10:70382529-70382962 | Common:5; Rare:150 |