| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53377854-53377982 | Rare:38 | ||||
| chr4:53378002-53378129 | Rare:39 | ||||
| chr4:53591481-53591592 | Rare:18 | ||||
| chr4:54064014-54064115 | Common:1; Rare:24 | ||||
| chr4:54064467-54064892 | Common:5; Rare:136 | ||||
| chr4:54099392-54099508 | Rare:18 | ||||
| chr4:55346115-55346419 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr4:55346505-55346776 | Common:2; Rare:89 | ||||
| chr4:55395513-55395672 | Rare:43 | ||||
| chr4:55395693-55396200 | Common:6; Rare:172; Clinvar:2 | ||||
| chr4:55396442-55396503 | Common:1; Rare:21 | ||||
| chr4:55545840-55546216 | Common:3; Rare:92 | ||||
| chr4:55546699-55546848 | Common:3; Rare:45 | ||||
| chr4:55546893-55547247 | Common:4; Rare:143 | ||||
| chr4:55853467-55853905 | Rare:117 |