| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:26091140-26091393 | Common:2; Rare:59 | ||||
| chr18:26226209-26226848 | Common:9; Rare:205 | ||||
| chr18:26460660-26460881 | Common:1; Rare:33 | ||||
| chr18:26549110-26549242 | Rare:29 | ||||
| chr18:26656972-26657145 | Common:5; Rare:63 | ||||
| chr18:31497868-31498044 | Rare:37 | ||||
| chr18:31498281-31498461 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:31658270-31658349 | Rare:13 | ||||
| chr18:31658890-31659129 | Common:2; Rare:43 | ||||
| chr18:31684222-31684438 | Common:1; Rare:62 | ||||
| chr18:31684455-31684875 | Common:1; Rare:125 | ||||
| chr18:31685165-31685693 | Common:6; Rare:168 | ||||
| chr18:31685900-31686070 | Common:1; Rare:50 | ||||
| chr18:31942312-31942522 | Common:1; Rare:54 | ||||
| chr18:31943027-31943480 | Common:7; Rare:141 |