| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46098538-46098632 | Rare:21 | ||||
| chr18:46098640-46098802 | Common:2; Rare:35 | ||||
| chr18:46104137-46104446 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr18:46104577-46104733 | Common:2; Rare:27 | ||||
| chr18:46104740-46104816 | Common:1; Rare:18 | ||||
| chr18:46173339-46173688 | Common:2; Rare:77 | ||||
| chr18:46173775-46174197 | Common:3; Rare:104 | ||||
| chr18:46333628-46333681 | Rare:15 | ||||
| chr18:46333862-46334136 | Common:1; Rare:64 | ||||
| chr18:46334222-46334371 | Rare:38 | ||||
| chr18:46601016-46601165 | Rare:21 | ||||
| chr18:46601349-46601504 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr18:46756923-46756978 | Rare:14 | ||||
| chr18:46756993-46757166 | Common:3; Rare:43 | ||||
| chr18:46757449-46757548 | Common:4; Rare:19 |