| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:104338670-104338847 | Rare:37 | ||||
| chr10:110005743-110005993 | Common:1; Rare:54 | ||||
| chr10:110006011-110006131 | Common:2; Rare:30 | ||||
| chr10:110007713-110008017 | Rare:87 | ||||
| chr10:110008153-110008284 | Common:1; Rare:60 | ||||
| chr10:110121217-110121413 | Common:2; Rare:35 | ||||
| chr10:110304750-110304800 | Rare:15 | ||||
| chr10:110304890-110305069 | Common:2; Rare:63 | ||||
| chr10:110497331-110497427 | Rare:22 | ||||
| chr10:110497676-110497907 | Common:5; Rare:77 | ||||
| chr10:110502052-110502357 | Common:5; Rare:60 | ||||
| chr10:110871621-110872016 | Rare:135 | ||||
| chr10:110884234-110884412 | Rare:25 | ||||
| chr10:110905272-110905522 | Common:3; Rare:67 | ||||
| chr10:110919106-110919654 | Common:8; Rare:147; Clinvar:1; Clinvar (benign):1 |