| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76737194-76737716 | Common:6; Rare:221 | ||||
| chr17:76737852-76738121 | Common:4; Rare:76 | ||||
| chr17:77088530-77088863 | Common:2; Rare:89 | ||||
| chr17:77140567-77141038 | Common:5; Rare:163 | ||||
| chr17:77287802-77287958 | Rare:19 | ||||
| chr17:77450256-77450755 | Common:2; Rare:102 | ||||
| chr17:78128611-78128924 | Common:7; Rare:78 | ||||
| chr17:78130639-78130812 | Rare:32 | ||||
| chr17:78186972-78187434 | Common:3; Rare:167 | ||||
| chr17:78360069-78360487 | Common:3; Rare:113 | ||||
| chr17:78378420-78378706 | Common:1; Rare:93 | ||||
| chr17:78782213-78782603 | Common:9; Rare:124 | ||||
| chr17:78799766-78799937 | Common:1; Rare:25 | ||||
| chr17:78840731-78841096 | Common:2; Rare:139 | ||||
| chr17:79009713-79009930 | Common:9; Rare:64; Clinvar:2; Clinvar (benign):1 |