| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:104494883-104495192 | Common:3; Rare:66 | ||||
| chr4:105708636-105708849 | Common:1; Rare:71 | ||||
| chr4:106316151-106316625 | Common:5; Rare:154 | ||||
| chr4:107720175-107720505 | Common:7; Rare:132 | ||||
| chr4:107989663-107989949 | Common:6; Rare:122; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108167702-108167859 | Rare:56 | ||||
| chr4:108168688-108168912 | Common:1; Rare:48 | ||||
| chr4:108620367-108620739 | Common:6; Rare:161 | ||||
| chr4:109433757-109433977 | Common:1; Rare:74 | ||||
| chr4:109703412-109703497 | Rare:31 | ||||
| chr4:109730063-109730212 | Common:2; Rare:31 | ||||
| chr4:109815465-109815817 | Common:1; Rare:92 | ||||
| chr4:110198535-110198798 | Rare:76 | ||||
| chr4:112231576-112231854 | Common:2; Rare:88 | ||||
| chr4:112231941-112232276 | Common:3; Rare:108 |