| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:1048878-1049086 | Common:2; Rare:110 | ||||
| chr10:3785251-3785551 | Common:4; Rare:102 | ||||
| chr10:6202780-6202936 | Common:4; Rare:40 | ||||
| chr10:7787950-7788226 | Common:1; Rare:114 | ||||
| chr10:12195792-12196234 | Rare:116 | ||||
| chr10:13099941-13100259 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300044-13300189 | Rare:52; Clinvar:1 | ||||
| chr10:13707566-13707761 | Common:1; Rare:43 | ||||
| chr10:14838018-14838341 | Common:2; Rare:85 | ||||
| chr10:14878637-14878901 | Common:2; Rare:79 | ||||
| chr10:14954030-14954153 | Rare:38 | ||||
| chr10:15097301-15097378 | Common:1; Rare:37 | ||||
| chr10:15860474-15860589 | Rare:32 | ||||
| chr10:17228468-17228675 | Common:1; Rare:57 | ||||
| chr10:17228782-17229026 | Common:3; Rare:63 |