| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23917648-23918025 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr3:24494126-24494317 | Rare:40 | ||||
| chr3:24495158-24495407 | Common:4; Rare:61 | ||||
| chr3:25428106-25428391 | Rare:64 | ||||
| chr3:25783360-25783621 | Common:2; Rare:94; Clinvar (benign):3 | ||||
| chr3:25789961-25790118 | Common:4; Rare:62 | ||||
| chr3:28241441-28241748 | Common:2; Rare:104 | ||||
| chr3:28348612-28348741 | Rare:30 | ||||
| chr3:28348770-28349185 | Common:3; Rare:134 | ||||
| chr3:29280831-29281102 | Common:3; Rare:55 | ||||
| chr3:30606292-30606630 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:31532380-31532648 | Common:3; Rare:73 | ||||
| chr3:31981634-31981722 | Rare:20 | ||||
| chr3:32570666-32570958 | Common:1; Rare:128 | ||||
| chr3:33277325-33277489 | Common:1; Rare:42 |