| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173530145-173530544 | Common:3; Rare:82 | ||||
| chr4:174283601-174283972 | Common:1; Rare:76 | ||||
| chr4:174284262-174284391 | Common:1; Rare:29 | ||||
| chr4:174522100-174522237 | Common:4; Rare:27 | ||||
| chr4:174522271-174522626 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522688-174522856 | Common:1; Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:174522858-174523056 | Rare:29; Clinvar (benign):1 | ||||
| chr4:176065733-176066001 | Common:7; Rare:86 | ||||
| chr4:176195558-176195694 | Common:1; Rare:50 | ||||
| chr4:176277404-176277710 | Common:2; Rare:41 | ||||
| chr4:176319721-176320070 | Common:5; Rare:117 | ||||
| chr4:177442376-177442530 | Rare:93; Clinvar:2 | ||||
| chr4:182448675-182449082 | Common:4; Rare:127 | ||||
| chr4:182917319-182917554 | Common:4; Rare:80 | ||||
| chr4:183099001-183099151 | Common:1; Rare:55 |