| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:54847076-54847338 | Common:2; Rare:37 | ||||
| chr16:54848247-54848380 | Common:2; Rare:32 | ||||
| chr16:55586943-55587077 | Common:1; Rare:22 | ||||
| chr16:56108851-56108987 | Common:2; Rare:15 | ||||
| chr16:56189566-56189610 | Rare:8 | ||||
| chr16:56194508-56194636 | Common:1; Rare:30 | ||||
| chr16:56300490-56300592 | Rare:12 | ||||
| chr16:56514642-56514717 | Rare:21; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:56823611-56823828 | Rare:75 | ||||
| chr16:57226648-57226810 | Common:1; Rare:22 | ||||
| chr16:57663310-57663476 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr16:58195057-58195262 | Common:1; Rare:36 | ||||
| chr16:58401415-58401667 | Rare:59 | ||||
| chr16:58542254-58542561 | Rare:64 | ||||
| chr16:58630452-58630502 | Common:1; Rare:5 |