| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36828725-36829131 | Common:3; Rare:151 | ||||
| chr18:46104225-46104408 | Common:3; Rare:50 | ||||
| chr18:46917412-46917611 | Rare:78 | ||||
| chr18:48538947-48539217 | Common:1; Rare:63 | ||||
| chr18:49813821-49814110 | Common:1; Rare:122 | ||||
| chr18:50879007-50879277 | Common:4; Rare:87 | ||||
| chr18:51030048-51030279 | Rare:81; Clinvar:3 | ||||
| chr18:51196902-51196957 | Rare:22 | ||||
| chr18:54224507-54224579 | Rare:13 | ||||
| chr18:54357856-54358023 | Common:6; Rare:51 | ||||
| chr18:55322350-55322419 | Rare:6 | ||||
| chr18:57803258-57803420 | Common:3; Rare:38 | ||||
| chr18:58580755-58581009 | Rare:46 | ||||
| chr18:59359006-59359182 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:59899847-59900073 | Common:3; Rare:70 |