| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:32801890-32802129 | Rare:60; Clinvar:2 | ||||
| chr22:33873188-33873339 | Common:3; Rare:44 | ||||
| chr22:35299733-35299977 | Common:2; Rare:65 | ||||
| chr22:35615568-35615797 | Common:4; Rare:43 | ||||
| chr22:35617071-35617080 | Rare:1 | ||||
| chr22:35617157-35617628 | Rare:117 | ||||
| chr22:36252958-36253179 | Rare:45 | ||||
| chr22:36387836-36388322 | Common:2; Rare:128; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36529077-36529531 | Common:6; Rare:142 | ||||
| chr22:37019423-37019768 | Common:5; Rare:99 | ||||
| chr22:37560338-37560558 | Common:1; Rare:77 | ||||
| chr22:37608911-37609052 | Common:1; Rare:42 | ||||
| chr22:37675568-37675710 | Common:1; Rare:39 | ||||
| chr22:37849316-37849480 | Rare:93 | ||||
| chr22:37953594-37953802 | Rare:81 |