| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14648168-14648252 | Rare:12 | ||||
| chr10:14659798-14660172 | Common:4; Rare:81 | ||||
| chr10:14926803-14926951 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:14942182-14942247 | Rare:18 | ||||
| chr10:15167849-15167967 | Rare:23 | ||||
| chr10:16799688-16799908 | Common:1; Rare:56 | ||||
| chr10:16891611-16891906 | Common:11; Rare:85 | ||||
| chr10:17511403-17511593 | Rare:35 | ||||
| chr10:17559410-17559548 | Rare:36 | ||||
| chr10:17585034-17585324 | Common:6; Rare:56 | ||||
| chr10:18399190-18399513 | Common:2; Rare:61 | ||||
| chr10:20003865-20004038 | Common:2; Rare:39 | ||||
| chr10:21495738-21496028 | Common:3; Rare:119 | ||||
| chr10:21527172-21527390 | Rare:73 | ||||
| chr10:21527513-21527603 | Rare:15 |