| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74737139-74737268 | Rare:45 | ||||
| chr17:74748386-74748716 | Common:4; Rare:119 | ||||
| chr17:74776281-74776543 | Common:4; Rare:87 | ||||
| chr17:75012565-75012688 | Common:1; Rare:31 | ||||
| chr17:75046929-75047171 | Common:1; Rare:74 | ||||
| chr17:75109870-75110010 | Common:1; Rare:42 | ||||
| chr17:75131502-75131810 | Common:4; Rare:131 | ||||
| chr17:75205360-75205730 | Common:1; Rare:112 | ||||
| chr17:75261580-75261939 | Common:4; Rare:113; Clinvar (benign):2 | ||||
| chr17:75271146-75271369 | Common:2; Rare:42 | ||||
| chr17:75289372-75289606 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393824-75393999 | Common:1; Rare:48 | ||||
| chr17:75456456-75456656 | Rare:54 | ||||
| chr17:75515416-75515644 | Common:3; Rare:66 | ||||
| chr17:75516398-75516563 | Rare:48; Clinvar (pathogenic):1 |