| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17966841-17967241 | Rare:163 | ||||
| chr19:18000590-18001750 | Common:27; Rare:878 | ||||
| chr19:18006850-18007288 | Common:12; Rare:219 | ||||
| chr19:18007999-18008172 | Common:5; Rare:65 | ||||
| chr19:18097480-18097880 | Common:2; Rare:180 | ||||
| chr19:18098642-18099042 | Rare:84 | ||||
| chr19:18099210-18099530 | Rare:64 | ||||
| chr19:18109530-18110040 | Common:7; Rare:203 | ||||
| chr19:18110280-18110810 | Common:6; Rare:180 | ||||
| chr19:18152220-18153330 | Common:15; Rare:1215 | ||||
| chr19:18153548-18153972 | Common:4; Rare:193 | ||||
| chr19:18161197-18161801 | Common:12; Rare:510; Clinvar (benign):10 | ||||
| chr19:18173523-18173926 | Common:5; Rare:248 | ||||
| chr19:18173879-18174279 | Common:1; Rare:147 | ||||
| chr19:18174360-18174690 | Common:1; Rare:99 |