| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12043171-12043318 | Common:2; Rare:41 | ||||
| chr10:12068758-12069018 | Common:2; Rare:99 | ||||
| chr10:12129456-12129733 | Rare:111 | ||||
| chr10:12195797-12196248 | Rare:124 | ||||
| chr10:13099695-13099900 | Rare:49 | ||||
| chr10:13099941-13100255 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13161304-13161590 | Common:1; Rare:75 | ||||
| chr10:13300040-13300179 | Rare:52; Clinvar:1 | ||||
| chr10:13348017-13348312 | Rare:94 | ||||
| chr10:14330807-14330998 | Rare:36 | ||||
| chr10:14838023-14838386 | Common:2; Rare:103 | ||||
| chr10:14878637-14878901 | Common:2; Rare:79 | ||||
| chr10:14954017-14954153 | Rare:46 | ||||
| chr10:14959289-14959369 | Rare:22 | ||||
| chr10:14959738-14960026 | Common:1; Rare:71 |