| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:812120-812472 | Common:4; Rare:129 | ||||
| chr18:812504-812620 | Common:1; Rare:28 | ||||
| chr18:812741-812900 | Rare:42 | ||||
| chr18:2571453-2571604 | Rare:47 | ||||
| chr18:2655543-2656183 | Common:9; Rare:240; Clinvar:5; Clinvar (benign):1 | ||||
| chr18:2982838-2983169 | Common:3; Rare:54 | ||||
| chr18:3247311-3247556 | Common:2; Rare:72 | ||||
| chr18:3261801-3262236 | Common:6; Rare:137 | ||||
| chr18:3448161-3448472 | Common:1; Rare:78 | ||||
| chr18:3449402-3449751 | Common:2; Rare:89 | ||||
| chr18:3450059-3450389 | Common:1; Rare:92 | ||||
| chr18:3451466-3451689 | Common:2; Rare:83 | ||||
| chr18:5543982-5544099 | Common:1; Rare:32 | ||||
| chr18:9102519-9102796 | Common:1; Rare:117; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136479-9137358 | Common:4; Rare:332 |