| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22168907-22169144 | Common:4; Rare:53 | ||||
| chr18:22169345-22169608 | Common:1; Rare:68 | ||||
| chr18:22169825-22170003 | Common:1; Rare:33 | ||||
| chr18:22933254-22933446 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933811-22933916 | Common:1; Rare:40 | ||||
| chr18:23453063-23453359 | Rare:103 | ||||
| chr18:23503308-23503547 | Common:2; Rare:88 | ||||
| chr18:24397754-24398102 | Common:2; Rare:121 | ||||
| chr18:24426560-24426781 | Common:4; Rare:90 | ||||
| chr18:25351020-25351129 | Rare:38 | ||||
| chr18:25352092-25352417 | Common:2; Rare:133 | ||||
| chr18:26090067-26090199 | Rare:50 | ||||
| chr18:26090525-26090978 | Common:5; Rare:173 | ||||
| chr18:28176968-28177314 | Common:3; Rare:165 | ||||
| chr18:31042738-31042907 | Common:1; Rare:26 |