| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12068662-12069018 | Common:2; Rare:124 | ||||
| chr10:12129458-12129733 | Rare:111 | ||||
| chr10:12195791-12196015 | Rare:57 | ||||
| chr10:13099929-13100188 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:13300058-13300215 | Rare:53; Clinvar:1 | ||||
| chr10:13301827-13302206 | Common:2; Rare:85 | ||||
| chr10:13302384-13302659 | Rare:51 | ||||
| chr10:14522002-14522036 | Rare:11 | ||||
| chr10:14604245-14604543 | Common:4; Rare:131 | ||||
| chr10:14838046-14838318 | Common:2; Rare:74 | ||||
| chr10:14878684-14878878 | Common:2; Rare:49 | ||||
| chr10:14954023-14954198 | Rare:62 | ||||
| chr10:15097211-15097396 | Common:3; Rare:89 | ||||
| chr10:16817361-16817736 | Common:4; Rare:133 | ||||
| chr10:17228940-17229438 | Common:5; Rare:112 |