| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46916880-46916949 | Rare:16 | ||||
| chr18:46917269-46917645 | Common:3; Rare:155 | ||||
| chr18:46917699-46917812 | Common:3; Rare:23 | ||||
| chr18:46946652-46946845 | Common:1; Rare:50 | ||||
| chr18:47150074-47150306 | Common:2; Rare:75 | ||||
| chr18:47150322-47150989 | Common:5; Rare:194 | ||||
| chr18:47176079-47176104 | Rare:3 | ||||
| chr18:47176279-47176416 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr18:47930046-47930150 | Rare:36 | ||||
| chr18:47930180-47930330 | Rare:60 | ||||
| chr18:47930749-47931034 | Rare:97 | ||||
| chr18:47931049-47931453 | Common:3; Rare:146 | ||||
| chr18:48538847-48539204 | Common:1; Rare:78 | ||||
| chr18:48539654-48539726 | Rare:21 | ||||
| chr18:48539926-48539971 | Rare:4 |