| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110776460-110776790 | Rare:84 | ||||
| chr12:110887895-110888295 | Rare:94 | ||||
| chr12:110906560-110906960 | Common:7; Rare:102 | ||||
| chr12:110913023-110913285 | Common:4; Rare:81; Clinvar:9; Clinvar (benign):12 | ||||
| chr12:111093458-111093728 | Rare:56 | ||||
| chr12:111111648-111112048 | Common:4; Rare:116 | ||||
| chr12:111355116-111355516 | Common:6; Rare:85 | ||||
| chr12:111402799-111403199 | Rare:153 | ||||
| chr12:111403364-111403577 | Rare:54 | ||||
| chr12:111403684-111404559 | Common:7; Rare:161 | ||||
| chr12:111404540-111405414 | Common:10; Rare:310 | ||||
| chr12:111406837-111407335 | Common:2; Rare:112 | ||||
| chr12:111410092-111410573 | Rare:97 | ||||
| chr12:111411194-111412170 | Common:9; Rare:220 | ||||
| chr12:111412270-111412986 | Common:1; Rare:137 |