| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:58671163-58671641 | Common:8; Rare:344; Clinvar:1; Clinvar (benign):2 | ||||
| chr18:58671880-58672370 | Common:4; Rare:206 | ||||
| chr18:59139689-59140005 | Common:5; Rare:143 | ||||
| chr18:59358270-59358940 | Common:4; Rare:223 | ||||
| chr18:59359128-59359520 | Common:8; Rare:334; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:62186919-62187363 | Common:11; Rare:233 | ||||
| chr18:62522785-62523436 | Common:18; Rare:446 | ||||
| chr18:62526690-62527060 | Common:10; Rare:253 | ||||
| chr18:62715321-62715579 | Common:4; Rare:140 | ||||
| chr18:63319950-63320350 | Common:1; Rare:111 | ||||
| chr18:63367156-63367360 | Common:2; Rare:130 | ||||
| chr18:63367526-63367634 | Common:5; Rare:38 | ||||
| chr18:63422358-63422669 | Common:1; Rare:144 | ||||
| chr18:68714982-68715357 | Common:13; Rare:278 | ||||
| chr18:69400758-69401023 | Common:8; Rare:175 |