| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50288270-50288490 | Common:2; Rare:41 | ||||
| chr18:50374868-50375158 | Common:6; Rare:161 | ||||
| chr18:50878390-50878720 | Common:6; Rare:117 | ||||
| chr18:50878935-50879249 | Common:8; Rare:197 | ||||
| chr18:50967865-50968063 | Rare:128 | ||||
| chr18:51030020-51030282 | Rare:180; Clinvar:5 | ||||
| chr18:51030638-51030898 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:51196040-51196640 | Rare:302 | ||||
| chr18:51197494-51197625 | Rare:45 | ||||
| chr18:51197550-51198120 | Rare:184 | ||||
| chr18:54223550-54224440 | Common:8; Rare:277 | ||||
| chr18:54224451-54224827 | Common:2; Rare:193 | ||||
| chr18:54269110-54269830 | Common:11; Rare:288 | ||||
| chr18:54269870-54270470 | Common:4; Rare:174 | ||||
| chr18:54357787-54358014 | Common:13; Rare:103 |