| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50281355-50281583 | Common:1; Rare:71 | ||||
| chr18:50281683-50281909 | Common:1; Rare:76 | ||||
| chr18:50287620-50287829 | Rare:75 | ||||
| chr18:50374837-50375181 | Common:5; Rare:106 | ||||
| chr18:50375270-50375383 | Rare:24 | ||||
| chr18:50559942-50560123 | Common:3; Rare:62 | ||||
| chr18:50878434-50878627 | Common:2; Rare:39 | ||||
| chr18:50878791-50879258 | Common:5; Rare:149 | ||||
| chr18:50967560-50967835 | Common:1; Rare:53 | ||||
| chr18:50967858-50968275 | Common:1; Rare:136 | ||||
| chr18:50968405-50968568 | Rare:42 | ||||
| chr18:51028241-51028416 | Common:2; Rare:27 | ||||
| chr18:51029626-51029734 | Rare:16 | ||||
| chr18:51029744-51030308 | Common:1; Rare:149; Clinvar:3 | ||||
| chr18:51030575-51030767 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):4 |