| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50374839-50375176 | Common:5; Rare:106 | ||||
| chr18:50559890-50560203 | Common:4; Rare:92 | ||||
| chr18:50878825-50879231 | Common:4; Rare:133 | ||||
| chr18:50967846-50968097 | Rare:86 | ||||
| chr18:50968194-50968264 | Rare:18 | ||||
| chr18:51029607-51029765 | Rare:22 | ||||
| chr18:51029953-51030308 | Rare:110; Clinvar:3 | ||||
| chr18:51030574-51030799 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):4 | ||||
| chr18:51196532-51196573 | Rare:9 | ||||
| chr18:51196920-51197018 | Rare:48 | ||||
| chr18:51197409-51198137 | Rare:224 | ||||
| chr18:54224240-54224263 | Rare:3 | ||||
| chr18:54224443-54224874 | Common:1; Rare:118 | ||||
| chr18:54269343-54269909 | Common:6; Rare:193 | ||||
| chr18:54270017-54270089 | Common:1; Rare:18 |