| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50374876-50375150 | Common:4; Rare:88 | ||||
| chr18:50878984-50879228 | Common:4; Rare:79 | ||||
| chr18:54357848-54357961 | Common:4; Rare:33 | ||||
| chr18:57621713-57621966 | Common:3; Rare:91 | ||||
| chr18:59139732-59139937 | Common:2; Rare:54 | ||||
| chr18:59899849-59900021 | Common:3; Rare:54 | ||||
| chr18:62186987-62187320 | Common:5; Rare:95 | ||||
| chr18:63422370-63422643 | Common:1; Rare:72 | ||||
| chr18:68714987-68715209 | Common:3; Rare:96 | ||||
| chr18:74148291-74148557 | Common:2; Rare:103 | ||||
| chr18:74291906-74292290 | Common:5; Rare:114 | ||||
| chr18:74496029-74496423 | Common:4; Rare:127 | ||||
| chr18:74597826-74597878 | Common:1; Rare:10 | ||||
| chr18:79988371-79988640 | Common:3; Rare:102; Clinvar (pathogenic):1 | ||||
| chr19:344784-344974 | Common:3; Rare:70 |