| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:267977-268152 | Common:1; Rare:72 | ||||
| chr18:658261-658292 | Rare:9 | ||||
| chr18:658312-658414 | Common:1; Rare:19 | ||||
| chr18:712591-712812 | Common:1; Rare:82 | ||||
| chr18:812216-812406 | Common:1; Rare:70 | ||||
| chr18:812545-812610 | Common:1; Rare:13 | ||||
| chr18:812751-812886 | Rare:34 | ||||
| chr18:2571402-2571635 | Common:1; Rare:67 | ||||
| chr18:3247326-3247536 | Common:1; Rare:58 | ||||
| chr18:3261811-3262211 | Common:6; Rare:132 | ||||
| chr18:3449949-3450301 | Common:1; Rare:101 | ||||
| chr18:3451461-3451709 | Common:2; Rare:86 | ||||
| chr18:7117735-7118094 | Common:7; Rare:98 | ||||
| chr18:9102484-9102772 | Common:2; Rare:117; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136542-9136837 | Rare:118 |