| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102831159-102831241 | Common:1; Rare:14 | ||||
| chr10:102837050-102837623 | Common:6; Rare:154; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr10:102837630-102837769 | Common:1; Rare:19 | ||||
| chr10:102854097-102854340 | Common:1; Rare:98 | ||||
| chr10:102854469-102854524 | Rare:16 | ||||
| chr10:102869319-102869418 | Rare:30 | ||||
| chr10:102869421-102869840 | Common:9; Rare:110 | ||||
| chr10:102917995-102918332 | Common:1; Rare:108 | ||||
| chr10:103094378-103094673 | Common:1; Rare:64 | ||||
| chr10:103193243-103193354 | Common:5; Rare:38; Clinvar (benign):1 | ||||
| chr10:103367870-103367981 | Common:2; Rare:17 | ||||
| chr10:103396386-103396722 | Rare:120 | ||||
| chr10:103452207-103452244 | Rare:7 | ||||
| chr10:103452262-103452453 | Rare:56 | ||||
| chr10:103917462-103917911 | Rare:110 |