| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827663-102828299 | Common:6; Rare:202 | ||||
| chr4:102868826-102869068 | Common:2; Rare:84 | ||||
| chr4:105708636-105708847 | Common:1; Rare:69 | ||||
| chr4:106316178-106316617 | Common:5; Rare:142 | ||||
| chr4:107720165-107720493 | Common:7; Rare:133 | ||||
| chr4:107824605-107824735 | Rare:29 | ||||
| chr4:107989675-107989935 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620367-108620710 | Common:6; Rare:156 | ||||
| chr4:110198509-110198721 | Rare:59 | ||||
| chr4:112231603-112231879 | Common:2; Rare:83 | ||||
| chr4:112285823-112285998 | Rare:54 | ||||
| chr4:112636860-112637187 | Common:1; Rare:91 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:113761129-113761276 | Common:1; Rare:35 | ||||
| chr4:113979602-113979817 | Common:6; Rare:49 |