| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74597566-74597914 | Common:2; Rare:93 | ||||
| chr18:75208496-75208631 | Common:2; Rare:35 | ||||
| chr18:75210728-75210911 | Common:4; Rare:49; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:77087440-77087684 | Common:7; Rare:61 | ||||
| chr18:77250970-77251027 | Rare:18 | ||||
| chr18:79679269-79679560 | Common:1; Rare:144 | ||||
| chr18:79988262-79988642 | Common:3; Rare:124; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344790-344933 | Common:3; Rare:47 | ||||
| chr19:409059-409287 | Common:2; Rare:75 | ||||
| chr19:507382-507512 | Common:2; Rare:41 | ||||
| chr19:572259-572649 | Common:3; Rare:202 | ||||
| chr19:633481-633745 | Common:8; Rare:122 | ||||
| chr19:663126-663426 | Common:3; Rare:117 | ||||
| chr19:680452-680797 | Common:2; Rare:123 | ||||
| chr19:821923-822077 | Rare:38 |