| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12129471-12129726 | Rare:106 | ||||
| chr10:12195770-12195975 | Rare:49 | ||||
| chr10:13099754-13099814 | Rare:22 | ||||
| chr10:13099949-13100283 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300044-13300160 | Rare:44; Clinvar:1 | ||||
| chr10:13348023-13348310 | Rare:94 | ||||
| chr10:14838039-14838398 | Common:4; Rare:102 | ||||
| chr10:14878606-14878882 | Common:2; Rare:88 | ||||
| chr10:14954023-14954187 | Rare:56 | ||||
| chr10:15097301-15097385 | Common:1; Rare:42 | ||||
| chr10:15860455-15860573 | Rare:34 | ||||
| chr10:17228463-17228675 | Common:1; Rare:57 | ||||
| chr10:17228964-17229026 | Common:1; Rare:17 | ||||
| chr10:17230554-17230718 | Rare:70; Clinvar:1 | ||||
| chr10:17643871-17644265 | Common:2; Rare:119 |