| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73568891-73569085 | Common:1; Rare:25 | ||||
| chr14:73569202-73569303 | Rare:30 | ||||
| chr14:73592069-73592176 | Common:2; Rare:40 | ||||
| chr14:73644533-73644605 | Rare:9 | ||||
| chr14:73644874-73645042 | Common:3; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73713931-73714063 | Common:1; Rare:36 | ||||
| chr14:73714316-73714511 | Common:2; Rare:74 | ||||
| chr14:73760301-73760409 | Common:1; Rare:20 | ||||
| chr14:73787121-73787379 | Common:2; Rare:88 | ||||
| chr14:73851715-73852009 | Common:5; Rare:94 | ||||
| chr14:73950167-73950333 | Common:3; Rare:74; Clinvar (benign):1 | ||||
| chr14:74019184-74019436 | Common:2; Rare:98 | ||||
| chr14:74084403-74084741 | Common:7; Rare:83 | ||||
| chr14:74302915-74303137 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr14:74493268-74493781 | Common:4; Rare:162; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 |