| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11851300-11851482 | Common:2; Rare:65 | ||||
| chr18:12307145-12307385 | Common:2; Rare:53 | ||||
| chr18:12308143-12308284 | Common:3; Rare:64 | ||||
| chr18:12702662-12703068 | Common:2; Rare:156 | ||||
| chr18:12884156-12884430 | Common:4; Rare:134 | ||||
| chr18:12947696-12948031 | Common:2; Rare:75 | ||||
| chr18:13611014-13611505 | Common:2; Rare:96 | ||||
| chr18:13612336-13612622 | Common:2; Rare:66 | ||||
| chr18:13726536-13726720 | Common:3; Rare:68 | ||||
| chr18:21111600-21112136 | Common:3; Rare:166 | ||||
| chr18:21600629-21600856 | Rare:53 | ||||
| chr18:21612194-21612352 | Common:1; Rare:45 | ||||
| chr18:21704754-21704917 | Rare:54 | ||||
| chr18:22933240-22933388 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr18:22933765-22933867 | Common:1; Rare:41 |