| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:812528-812578 | Rare:10 | ||||
| chr18:812741-812795 | Rare:19 | ||||
| chr18:904158-904451 | Common:1; Rare:63 | ||||
| chr18:2571413-2571593 | Rare:57 | ||||
| chr18:2655583-2655726 | Common:3; Rare:72 | ||||
| chr18:2655825-2655973 | Common:1; Rare:46 | ||||
| chr18:3247332-3247877 | Common:1; Rare:150 | ||||
| chr18:3261811-3262233 | Common:6; Rare:135 | ||||
| chr18:3448223-3448431 | Common:1; Rare:48 | ||||
| chr18:3449177-3449345 | Common:5; Rare:42 | ||||
| chr18:3449864-3450206 | Rare:93 | ||||
| chr18:4455215-4455588 | Common:4; Rare:135 | ||||
| chr18:6414863-6414990 | Rare:49 | ||||
| chr18:7946790-7946946 | Rare:36 | ||||
| chr18:9102519-9102772 | Common:1; Rare:107; Clinvar:6; Clinvar (benign):2 |