| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63367075-63367353 | Common:1; Rare:103 | ||||
| chr18:63422377-63422711 | Common:2; Rare:96 | ||||
| chr18:68714987-68715271 | Common:6; Rare:125 | ||||
| chr18:70205659-70205774 | Common:3; Rare:48; Clinvar (benign):2 | ||||
| chr18:74597606-74597907 | Common:2; Rare:76 | ||||
| chr18:76822236-76822579 | Common:11; Rare:93 | ||||
| chr18:79988371-79988645 | Common:3; Rare:103; Clinvar (pathogenic):2 | ||||
| chr19:572322-572691 | Common:1; Rare:185 | ||||
| chr19:663123-663362 | Common:2; Rare:88 | ||||
| chr19:708794-709149 | Common:3; Rare:98 | ||||
| chr19:893167-893484 | Common:3; Rare:132 | ||||
| chr19:913144-913247 | Rare:34 | ||||
| chr19:984230-984348 | Rare:42 | ||||
| chr19:1132130-1132492 | Common:2; Rare:149 | ||||
| chr19:1269057-1269398 | Common:2; Rare:130 |