| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105552378-105552510 | Rare:21 | ||||
| chr4:105552519-105552880 | Common:1; Rare:75 | ||||
| chr4:105708628-105708877 | Common:3; Rare:81 | ||||
| chr4:105895304-105895515 | Rare:59 | ||||
| chr4:106316155-106316612 | Common:5; Rare:149 | ||||
| chr4:107720175-107720532 | Common:7; Rare:145 | ||||
| chr4:107824461-107824564 | Rare:18 | ||||
| chr4:107824603-107824762 | Rare:32 | ||||
| chr4:107989669-107989942 | Common:6; Rare:121; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620380-108620647 | Common:6; Rare:135 | ||||
| chr4:109433757-109433946 | Common:1; Rare:63 | ||||
| chr4:109815395-109815553 | Common:1; Rare:42 | ||||
| chr4:112231597-112231886 | Common:2; Rare:88 | ||||
| chr4:112285757-112285978 | Rare:70 | ||||
| chr4:112636892-112637187 | Common:1; Rare:79 |