| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31498062-31498259 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:32018680-32018860 | Common:2; Rare:52 | ||||
| chr18:32092366-32092756 | Common:5; Rare:176 | ||||
| chr18:35290178-35290384 | Common:2; Rare:73 | ||||
| chr18:35344394-35344516 | Common:2; Rare:41 | ||||
| chr18:35972472-35972719 | Common:3; Rare:79 | ||||
| chr18:36129229-36129520 | Common:4; Rare:90 | ||||
| chr18:36129767-36129935 | Common:1; Rare:67 | ||||
| chr18:36187419-36187516 | Common:1; Rare:40 | ||||
| chr18:36828736-36829150 | Common:3; Rare:158 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:47150432-47150546 | Common:3; Rare:44 | ||||
| chr18:49487138-49487328 | Common:3; Rare:77 | ||||
| chr18:49813500-49813602 | Rare:24 | ||||
| chr18:49813826-49814158 | Common:1; Rare:138 |