| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74291912-74292265 | Common:4; Rare:102 | ||||
| chr18:74496021-74496409 | Common:4; Rare:125 | ||||
| chr18:74597584-74597929 | Common:2; Rare:95 | ||||
| chr18:76822224-76822579 | Common:11; Rare:96 | ||||
| chr18:79988373-79988653 | Common:3; Rare:104; Clinvar (pathogenic):2 | ||||
| chr19:507266-507526 | Common:2; Rare:90 | ||||
| chr19:572248-572628 | Common:3; Rare:188 | ||||
| chr19:633478-633713 | Common:8; Rare:112 | ||||
| chr19:663153-663473 | Common:2; Rare:127 | ||||
| chr19:821913-822002 | Rare:17 | ||||
| chr19:893167-893312 | Common:2; Rare:40 | ||||
| chr19:984228-984348 | Common:1; Rare:43 | ||||
| chr19:1260935-1261173 | Common:3; Rare:79 | ||||
| chr19:1269057-1269381 | Common:2; Rare:122 | ||||
| chr19:1354793-1355017 | Common:1; Rare:103 |