| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3446808-3448606 | Common:39; Rare:1601 | ||||
| chr18:3448905-3449630 | Common:25; Rare:482 | ||||
| chr18:3449563-3449860 | Common:4; Rare:123 | ||||
| chr18:3449846-3450551 | Common:6; Rare:706; Clinvar (benign):2 | ||||
| chr18:3450789-3451958 | Common:17; Rare:719 | ||||
| chr18:3453347-3454529 | Common:13; Rare:457 | ||||
| chr18:3454819-3455180 | Rare:101 | ||||
| chr18:5294794-5295529 | Common:11; Rare:757 | ||||
| chr18:5295998-5296522 | Common:10; Rare:1228 | ||||
| chr18:5296780-5297240 | Common:9; Rare:332 | ||||
| chr18:6729252-6730150 | Common:77; Rare:868 | ||||
| chr18:7566300-7566780 | Common:3; Rare:105 | ||||
| chr18:7566960-7567442 | Common:11; Rare:311 | ||||
| chr18:8609164-8609564 | Common:4; Rare:248 | ||||
| chr18:8704930-8705686 | Common:8; Rare:871 |