| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119596556-119596712 | Common:1; Rare:38 | ||||
| chr10:119596833-119597282 | Common:3; Rare:116 | ||||
| chr10:119651165-119651436 | Common:6; Rare:100; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:119725767-119726117 | Common:3; Rare:123 | ||||
| chr10:119818435-119818800 | Rare:117 | ||||
| chr10:119819252-119819335 | Rare:9 | ||||
| chr10:119872800-119873039 | Common:4; Rare:89 | ||||
| chr10:119892484-119892777 | Common:3; Rare:106 | ||||
| chr10:120851199-120851506 | Common:6; Rare:112 | ||||
| chr10:121596620-121596920 | Common:2; Rare:65 | ||||
| chr10:121598393-121598613 | Common:1; Rare:77; Clinvar:1 | ||||
| chr10:121927883-121928225 | Common:2; Rare:104 | ||||
| chr10:121928433-121928525 | Rare:26 | ||||
| chr10:121974786-121974898 | Rare:42 | ||||
| chr10:121975125-121975332 | Common:1; Rare:44 |