| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54357706-54358076 | Common:11; Rare:112 | ||||
| chr18:55321754-55321921 | Rare:38 | ||||
| chr18:55401615-55401783 | Rare:36 | ||||
| chr18:55588038-55588271 | Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr18:55588492-55588502 | Rare:1 | ||||
| chr18:56651118-56651424 | Common:4; Rare:82 | ||||
| chr18:57621712-57621950 | Common:3; Rare:86 | ||||
| chr18:57802973-57803558 | Common:5; Rare:153; Clinvar:2; Clinvar (benign):3 | ||||
| chr18:58671244-58671424 | Rare:81 | ||||
| chr18:58862846-58863130 | Rare:60 | ||||
| chr18:58863525-58863617 | Common:1; Rare:22 | ||||
| chr18:58864801-58864894 | Rare:18 | ||||
| chr18:59358510-59358778 | Common:1; Rare:68 | ||||
| chr18:59359030-59359092 | Rare:30 | ||||
| chr18:59359237-59359517 | Common:3; Rare:119; Clinvar:1 |