| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173333498-173333878 | Common:2; Rare:98 | ||||
| chr4:173369744-173369943 | Common:1; Rare:66 | ||||
| chr4:173370690-173370982 | Common:2; Rare:74 | ||||
| chr4:174283612-174283965 | Common:1; Rare:71 | ||||
| chr4:174522271-174522592 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:176319670-176320091 | Common:5; Rare:130 | ||||
| chr4:176792264-176792484 | Common:1; Rare:64 | ||||
| chr4:177442331-177442521 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:182143869-182144057 | Rare:45 | ||||
| chr4:182144173-182144237 | Common:5; Rare:22 | ||||
| chr4:182144408-182144713 | Common:3; Rare:97 | ||||
| chr4:182917319-182917575 | Common:4; Rare:82 | ||||
| chr4:183099001-183099257 | Common:3; Rare:85 | ||||
| chr4:183444345-183444789 | Common:2; Rare:188 | ||||
| chr4:183504522-183504803 | Common:1; Rare:94 |