| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54449412-54449516 | Rare:34 | ||||
| chr19:54874072-54874284 | Common:2; Rare:50 | ||||
| chr19:55094348-55094703 | Rare:107 | ||||
| chr19:55153961-55154031 | Rare:13; Clinvar:1 | ||||
| chr19:55156199-55156678 | Common:5; Rare:157; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr19:55157560-55157927 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):3 | ||||
| chr19:55207233-55207365 | Common:1; Rare:47 | ||||
| chr19:55258482-55258677 | Common:3; Rare:74 | ||||
| chr19:55258988-55259241 | Common:1; Rare:84 | ||||
| chr19:55280038-55280157 | Rare:26 | ||||
| chr19:55385738-55385982 | Common:6; Rare:83 | ||||
| chr19:55599469-55599740 | Common:2; Rare:84 | ||||
| chr19:55600223-55600375 | Rare:69 | ||||
| chr19:55634897-55635059 | Common:1; Rare:40 | ||||
| chr19:55643428-55643666 | Common:3; Rare:77 |