| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979374-75979488 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr17:76027194-76027529 | Common:1; Rare:75 | ||||
| chr17:76072366-76072567 | Common:6; Rare:126 | ||||
| chr17:76103712-76103876 | Common:4; Rare:53 | ||||
| chr17:76141230-76141445 | Common:1; Rare:54 | ||||
| chr17:76265174-76265573 | Common:1; Rare:132 | ||||
| chr17:76384464-76384668 | Common:2; Rare:58 | ||||
| chr17:76493126-76493347 | Common:2; Rare:41 | ||||
| chr17:76501340-76501547 | Rare:67; Clinvar (benign):3 | ||||
| chr17:76726449-76726872 | Common:5; Rare:156 | ||||
| chr17:76737253-76737537 | Common:4; Rare:134 | ||||
| chr17:76737852-76738043 | Common:3; Rare:53 | ||||
| chr17:77089288-77089315 | Rare:12 | ||||
| chr17:77140661-77141054 | Common:2; Rare:137 | ||||
| chr17:77206572-77206867 | Common:1; Rare:71 |