| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119165399-119165744 | Common:4; Rare:124; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119178779-119178898 | Common:2; Rare:52 | ||||
| chr10:119596929-119597231 | Common:1; Rare:84 | ||||
| chr10:119651210-119651382 | Common:2; Rare:71 | ||||
| chr10:119818479-119818736 | Rare:85 | ||||
| chr10:119892610-119892779 | Common:2; Rare:65 | ||||
| chr10:120851281-120851438 | Common:1; Rare:66 | ||||
| chr10:121927890-121928200 | Common:2; Rare:93 | ||||
| chr10:121928433-121928529 | Rare:26 | ||||
| chr10:121974752-121974894 | Common:1; Rare:48 | ||||
| chr10:122375154-122375265 | Rare:39 | ||||
| chr10:122879531-122879690 | Common:3; Rare:44 | ||||
| chr10:122954185-122954508 | Common:1; Rare:119 | ||||
| chr10:123008764-123009055 | Common:6; Rare:87; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092369-124092511 | Rare:37 |