| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173334245-173334768 | Rare:135 | ||||
| chr4:173369802-173369971 | Common:1; Rare:57 | ||||
| chr4:173370668-173370976 | Common:2; Rare:78 | ||||
| chr4:173530196-173530471 | Common:2; Rare:60 | ||||
| chr4:174283573-174283983 | Common:1; Rare:81 | ||||
| chr4:174522012-174522710 | Common:7; Rare:190; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522796-174522814 | Rare:5 | ||||
| chr4:176319907-176320215 | Common:3; Rare:95 | ||||
| chr4:177309719-177309909 | Common:1; Rare:55 | ||||
| chr4:177442371-177442549 | Rare:106; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182917300-182917493 | Common:2; Rare:72 | ||||
| chr4:183444407-183444789 | Common:2; Rare:174 | ||||
| chr4:183504536-183504799 | Common:1; Rare:85 | ||||
| chr4:183659104-183659417 | Common:1; Rare:104 | ||||
| chr4:184474442-184474850 | Rare:87 |