| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:267994-268113 | Common:1; Rare:48 | ||||
| chr18:657529-657942 | Common:9; Rare:123 | ||||
| chr18:812211-812395 | Common:1; Rare:62 | ||||
| chr18:812521-812624 | Common:1; Rare:25 | ||||
| chr18:812741-812997 | Common:1; Rare:68 | ||||
| chr18:2571457-2571640 | Rare:53 | ||||
| chr18:2655589-2655887 | Common:4; Rare:123 | ||||
| chr18:3247340-3247937 | Common:1; Rare:173 | ||||
| chr18:3261801-3262236 | Common:6; Rare:137 | ||||
| chr18:3448200-3448496 | Common:1; Rare:70 | ||||
| chr18:3450019-3450213 | Common:1; Rare:56 | ||||
| chr18:5540400-5540534 | Rare:16 | ||||
| chr18:9102475-9102766 | Common:2; Rare:118; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136605-9136872 | Rare:104 | ||||
| chr18:9708055-9708408 | Common:4; Rare:93 |