| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:73529895-73529935 | Common:1; Rare:6 | ||||
| chr3:73530813-73531093 | Rare:62 | ||||
| chr3:73531678-73531931 | Rare:53 | ||||
| chr3:73552819-73552850 | Rare:6 | ||||
| chr3:73558744-73558773 | Rare:3 | ||||
| chr3:73560676-73560711 | Rare:7 | ||||
| chr3:73571524-73571561 | Rare:8 | ||||
| chr3:73572759-73573016 | Common:2; Rare:36 | ||||
| chr3:73577470-73577570 | Common:2; Rare:20 | ||||
| chr3:73580216-73580302 | Rare:11 | ||||
| chr3:75435003-75435392 | Common:6; Rare:131 | ||||
| chr3:75641093-75641403 | Common:1; Rare:47 | ||||
| chr3:80770318-80770742 | Common:9; Rare:120 | ||||
| chr3:88087204-88087481 | Rare:50 | ||||
| chr3:94050549-94050887 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 |