| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119596603-119596750 | Common:2; Rare:67 | ||||
| chr10:119596874-119597314 | Common:4; Rare:227 | ||||
| chr10:119651203-119651661 | Common:12; Rare:305; Clinvar:2; Clinvar (benign):14 | ||||
| chr10:119725716-119726202 | Common:8; Rare:315 | ||||
| chr10:119872804-119873103 | Common:8; Rare:200 | ||||
| chr10:119892490-119892783 | Common:6; Rare:202 | ||||
| chr10:120851146-120851448 | Common:9; Rare:185 | ||||
| chr10:121927907-121928292 | Common:3; Rare:173 | ||||
| chr10:121928342-121928564 | Rare:95 | ||||
| chr10:121974752-121974901 | Common:2; Rare:95 | ||||
| chr10:121975125-121975349 | Common:2; Rare:84 | ||||
| chr10:122112703-122113211 | Common:9; Rare:257 | ||||
| chr10:122331697-122331894 | Rare:85 | ||||
| chr10:122374358-122374795 | Common:3; Rare:232 | ||||
| chr10:122374914-122375273 | Common:2; Rare:237 |