| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:73481481-73481862 | Common:3; Rare:92 | ||||
| chr4:73987977-73988226 | Rare:71 | ||||
| chr4:74038683-74038908 | Rare:63 | ||||
| chr4:74157915-74158206 | Common:1; Rare:134 | ||||
| chr4:75514260-75514514 | Common:1; Rare:89 | ||||
| chr4:75514673-75514737 | Rare:18 | ||||
| chr4:75673273-75673692 | Common:1; Rare:160 | ||||
| chr4:75724357-75724819 | Common:2; Rare:138 | ||||
| chr4:76148357-76148586 | Common:4; Rare:71 | ||||
| chr4:76196024-76196142 | Common:1; Rare:22 | ||||
| chr4:76213531-76214025 | Common:4; Rare:173; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:76251606-76251739 | Rare:33 | ||||
| chr4:76306402-76306820 | Common:2; Rare:118 | ||||
| chr4:76586110-76586321 | Common:2; Rare:35 | ||||
| chr4:76898016-76898339 | Common:1; Rare:70 |