| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:77132014-77132245 | Common:2; Rare:68 | ||||
| chr18:77132653-77132860 | Common:1; Rare:63 | ||||
| chr18:79068827-79069532 | Common:12; Rare:289 | ||||
| chr18:79395823-79395958 | Rare:31 | ||||
| chr18:79400193-79400395 | Common:5; Rare:99 | ||||
| chr18:79400702-79400986 | Common:9; Rare:35 | ||||
| chr18:79679271-79679595 | Common:1; Rare:163 | ||||
| chr18:79679679-79679941 | Common:3; Rare:114 | ||||
| chr18:79950889-79950910 | Rare:7 | ||||
| chr18:79951623-79951909 | Common:4; Rare:110 | ||||
| chr18:79964535-79964705 | Common:1; Rare:54 | ||||
| chr18:79988084-79988236 | Rare:61 | ||||
| chr18:79988379-79988789 | Common:5; Rare:145; Clinvar (pathogenic):2 | ||||
| chr18:80033596-80033792 | Common:2; Rare:55 | ||||
| chr18:80034619-80034771 | Rare:55 |