| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:61894408-61894541 | Common:2; Rare:44 | ||||
| chr18:62186937-62187293 | Common:5; Rare:97 | ||||
| chr18:63367131-63367324 | Common:1; Rare:71 | ||||
| chr18:67516651-67516992 | Common:5; Rare:83 | ||||
| chr18:68714956-68715211 | Common:4; Rare:108 | ||||
| chr18:70205659-70205783 | Common:3; Rare:51; Clinvar (benign):2 | ||||
| chr18:74597601-74597910 | Common:2; Rare:82 | ||||
| chr18:75209056-75209428 | Common:3; Rare:106 | ||||
| chr18:76822233-76822616 | Common:11; Rare:107 | ||||
| chr18:79679333-79679560 | Common:1; Rare:109 | ||||
| chr18:79951608-79951808 | Common:2; Rare:100 | ||||
| chr18:79988489-79988667 | Common:3; Rare:69; Clinvar (pathogenic):2 | ||||
| chr19:572380-572628 | Rare:139 | ||||
| chr19:633505-633730 | Common:8; Rare:111 | ||||
| chr19:663175-663464 | Common:2; Rare:111 |