| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173530205-173530462 | Common:2; Rare:59 | ||||
| chr4:174283626-174283965 | Common:1; Rare:65 | ||||
| chr4:176319721-176320215 | Common:5; Rare:144 | ||||
| chr4:177442368-177442529 | Rare:97; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143781-182144040 | Common:2; Rare:62 | ||||
| chr4:182144435-182144734 | Common:3; Rare:97 | ||||
| chr4:183099016-183099285 | Common:2; Rare:88 | ||||
| chr4:183444407-183444774 | Common:2; Rare:172 | ||||
| chr4:183659160-183659377 | Common:1; Rare:69 | ||||
| chr4:184649403-184649805 | Common:4; Rare:131 | ||||
| chr4:184734017-184734196 | Common:4; Rare:95 | ||||
| chr4:185396431-185396843 | Rare:136 | ||||
| chr4:185425867-185426254 | Common:3; Rare:117 | ||||
| chr4:189940662-189940974 | Common:10; Rare:112 | ||||
| chr5:218112-218352 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):3 |