| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600430-21600775 | Rare:99 | ||||
| chr18:21612175-21612392 | Common:1; Rare:63 | ||||
| chr18:21612513-21612684 | Common:1; Rare:45 | ||||
| chr18:21703431-21703831 | Rare:154 | ||||
| chr18:21703792-21704527 | Common:3; Rare:277 | ||||
| chr18:21704757-21704940 | Rare:56 | ||||
| chr18:21740571-21740964 | Common:3; Rare:122 | ||||
| chr18:22933141-22933408 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:22933759-22933910 | Common:1; Rare:63 | ||||
| chr18:23135254-23135487 | Common:2; Rare:59 | ||||
| chr18:23437670-23438210 | Common:8; Rare:157 | ||||
| chr18:23453092-23453291 | Rare:58 | ||||
| chr18:23502760-23503200 | Common:1; Rare:97 | ||||
| chr18:23503246-23503541 | Common:2; Rare:112 | ||||
| chr18:23586402-23586589 | Common:3; Rare:89; Clinvar:3; Clinvar (benign):2 |