| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586397-23586531 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:25352098-25352438 | Common:2; Rare:138 | ||||
| chr18:32018401-32018728 | Common:2; Rare:87 | ||||
| chr18:32092378-32092721 | Common:5; Rare:157 | ||||
| chr18:34976942-34977058 | Common:1; Rare:20 | ||||
| chr18:35290193-35290384 | Common:2; Rare:68 | ||||
| chr18:35497958-35497985 | Rare:5 | ||||
| chr18:35972449-35972722 | Common:4; Rare:86 | ||||
| chr18:36129301-36129490 | Common:1; Rare:56 | ||||
| chr18:36828765-36829150 | Common:3; Rare:141 | ||||
| chr18:45967261-45967475 | Rare:76 | ||||
| chr18:46104136-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:49487192-49487356 | Common:3; Rare:64 | ||||
| chr18:49813832-49814128 | Common:1; Rare:124 | ||||
| chr18:50878963-50879228 | Common:4; Rare:88 |