| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35972449-35972717 | Common:4; Rare:84 | ||||
| chr18:36067425-36067708 | Common:2; Rare:100 | ||||
| chr18:36187414-36187525 | Common:2; Rare:42 | ||||
| chr18:36828748-36829141 | Common:3; Rare:146 | ||||
| chr18:45967247-45967442 | Rare:70 | ||||
| chr18:46098239-46098524 | Common:11; Rare:83; Clinvar (benign):5 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:47150450-47150570 | Common:3; Rare:43 | ||||
| chr18:49460621-49460832 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49490454-49490914 | Common:1; Rare:114 | ||||
| chr18:49561879-49562078 | Rare:51 | ||||
| chr18:49813826-49814080 | Common:1; Rare:109 | ||||
| chr18:50374917-50375137 | Common:2; Rare:67 | ||||
| chr18:50878954-50879215 | Common:4; Rare:88 | ||||
| chr18:54357794-54357903 | Common:3; Rare:38 |