| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:118046573-118047075 | Common:4; Rare:154 | ||||
| chr10:118342216-118342351 | Common:2; Rare:37 | ||||
| chr10:118754919-118755366 | Common:2; Rare:150 | ||||
| chr10:119029286-119029545 | Rare:86 | ||||
| chr10:119029613-119029719 | Rare:39 | ||||
| chr10:119030515-119030840 | Common:2; Rare:96 | ||||
| chr10:119080767-119081018 | Common:1; Rare:110 | ||||
| chr10:119103861-119104182 | Common:2; Rare:73 | ||||
| chr10:119165346-119165808 | Common:4; Rare:162; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:119178428-119178609 | Common:1; Rare:46 | ||||
| chr10:119178731-119179055 | Common:3; Rare:108 | ||||
| chr10:119207336-119207562 | Common:1; Rare:74 | ||||
| chr10:119542642-119542862 | Common:4; Rare:69 | ||||
| chr10:119596644-119596790 | Common:1; Rare:36 | ||||
| chr10:119596882-119597055 | Common:1; Rare:41 |