| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51073552-51073748 | Rare:43 | ||||
| chr18:51700431-51700521 | Rare:22 | ||||
| chr18:54110408-54110492 | Rare:19 | ||||
| chr18:54179044-54179069 | Common:1; Rare:6 | ||||
| chr18:54234943-54235021 | Rare:15 | ||||
| chr18:54270540-54270806 | Common:3; Rare:54 | ||||
| chr18:55234677-55234847 | Common:2; Rare:34; Clinvar (benign):2 | ||||
| chr18:55236254-55236463 | Common:5; Rare:37 | ||||
| chr18:55237188-55237411 | Rare:38 | ||||
| chr18:55244073-55244190 | Rare:24 | ||||
| chr18:55245991-55246202 | Rare:30 | ||||
| chr18:55253770-55253925 | Common:1; Rare:22 | ||||
| chr18:55259970-55260076 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:55261056-55261062 | |||||
| chr18:55263496-55263567 | Rare:12 |