| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:170090212-170090370 | Common:1; Rare:57 | ||||
| chr4:173334276-173334739 | Rare:117 | ||||
| chr4:173369809-173369935 | Common:1; Rare:43 | ||||
| chr4:173370681-173370962 | Common:2; Rare:71 | ||||
| chr4:174283611-174283965 | Common:1; Rare:72 | ||||
| chr4:177442371-177442519 | Rare:89; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143820-182143972 | Common:2; Rare:34 | ||||
| chr4:182144408-182144734 | Common:3; Rare:107 | ||||
| chr4:182243257-182243431 | Rare:35 | ||||
| chr4:183659072-183659401 | Common:1; Rare:106 | ||||
| chr4:184649413-184649805 | Common:4; Rare:127 | ||||
| chr4:184734117-184734419 | Common:6; Rare:90 | ||||
| chr4:185396581-185396851 | Rare:86 | ||||
| chr4:185425880-185426252 | Common:3; Rare:110 | ||||
| chr4:186723759-186723897 | Common:4; Rare:58 |