| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:9614827-9615156 | Common:2; Rare:87 | ||||
| chr18:9707910-9708500 | Common:7; Rare:145 | ||||
| chr18:9913901-9914070 | Common:1; Rare:65 | ||||
| chr18:9914711-9915113 | Common:12; Rare:225 | ||||
| chr18:10454513-10454670 | Rare:56 | ||||
| chr18:10525851-10526099 | Common:2; Rare:99 | ||||
| chr18:11689247-11689660 | Common:6; Rare:184; Clinvar:4 | ||||
| chr18:11690090-11690550 | Common:5; Rare:95 | ||||
| chr18:11851251-11851446 | Common:1; Rare:69 | ||||
| chr18:11908220-11908423 | Rare:57 | ||||
| chr18:11980846-11981026 | Common:4; Rare:57 | ||||
| chr18:11981280-11981581 | Common:4; Rare:85 | ||||
| chr18:12308085-12308309 | Common:3; Rare:96 | ||||
| chr18:12376726-12376958 | Rare:76; Clinvar (benign):1 | ||||
| chr18:12377207-12377871 | Common:7; Rare:184; Clinvar (benign):3 |