| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49813510-49813617 | Rare:22 | ||||
| chr18:49813826-49814206 | Common:1; Rare:158 | ||||
| chr18:50281436-50281847 | Common:3; Rare:129 | ||||
| chr18:50374864-50375137 | Common:3; Rare:88 | ||||
| chr18:50878959-50879254 | Common:4; Rare:97 | ||||
| chr18:51030048-51030222 | Rare:57 | ||||
| chr18:54224108-54224451 | Common:8; Rare:116 | ||||
| chr18:54269762-54269831 | Rare:18 | ||||
| chr18:54357866-54357993 | Common:6; Rare:40 | ||||
| chr18:54828359-54828628 | Rare:62 | ||||
| chr18:55401684-55401995 | Rare:57 | ||||
| chr18:55589723-55589996 | Common:2; Rare:88 | ||||
| chr18:56651132-56651439 | Common:4; Rare:81 | ||||
| chr18:57621707-57621972 | Common:3; Rare:93 | ||||
| chr18:57803041-57803261 | Common:1; Rare:63; Clinvar (benign):1 |