| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:117241113-117241997 | Common:8; Rare:516 | ||||
| chr10:117373766-117374210 | Common:8; Rare:168 | ||||
| chr10:117374679-117375650 | Common:23; Rare:957 | ||||
| chr10:117375814-117376278 | Common:6; Rare:141 | ||||
| chr10:118045941-118046414 | Common:2; Rare:228 | ||||
| chr10:118046428-118047164 | Common:21; Rare:699 | ||||
| chr10:118341761-118341896 | Rare:22 | ||||
| chr10:118342159-118342559 | Common:6; Rare:183 | ||||
| chr10:118753829-118754632 | Common:4; Rare:325 | ||||
| chr10:118754906-118755436 | Common:10; Rare:932 | ||||
| chr10:119029260-119029719 | Rare:312 | ||||
| chr10:119030110-119030781 | Common:4; Rare:393; Clinvar (pathogenic):1 | ||||
| chr10:119080693-119081036 | Common:6; Rare:554 | ||||
| chr10:119080954-119081354 | Common:2; Rare:79 | ||||
| chr10:119103784-119104219 | Common:7; Rare:230 |