| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12043171-12043466 | Common:2; Rare:95 | ||||
| chr10:12068782-12069023 | Common:2; Rare:93 | ||||
| chr10:12129472-12129726 | Rare:106 | ||||
| chr10:12195814-12196241 | Rare:115 | ||||
| chr10:12349734-12349826 | Common:1; Rare:35 | ||||
| chr10:13099710-13099839 | Rare:33 | ||||
| chr10:13099941-13100205 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:13300038-13300141 | Rare:42; Clinvar:1 | ||||
| chr10:14604247-14604543 | Common:4; Rare:130 | ||||
| chr10:14838016-14838386 | Common:2; Rare:104 | ||||
| chr10:14878637-14878897 | Common:2; Rare:78 | ||||
| chr10:14954017-14954174 | Rare:52 | ||||
| chr10:15097290-15097362 | Common:1; Rare:37 | ||||
| chr10:15860455-15860803 | Rare:88 | ||||
| chr10:17228901-17229026 | Common:3; Rare:30 |