| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:69495119-69495677 | Common:1; Rare:190 | ||||
| chr4:69495684-69496146 | Common:4; Rare:113 | ||||
| chr4:69760499-69760677 | Rare:31 | ||||
| chr4:70688214-70688613 | Common:2; Rare:108 | ||||
| chr4:70902202-70902382 | Common:4; Rare:67 | ||||
| chr4:70993482-70993658 | Common:4; Rare:52 | ||||
| chr4:71186983-71187339 | Common:2; Rare:101 | ||||
| chr4:73069642-73069886 | Common:1; Rare:115 | ||||
| chr4:73104073-73104386 | Common:1; Rare:62 | ||||
| chr4:73258530-73258913 | Common:1; Rare:115 | ||||
| chr4:73259124-73259232 | Rare:23 | ||||
| chr4:73397217-73397265 | Rare:6 | ||||
| chr4:73404046-73404421 | Rare:88; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr4:73409297-73409625 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:73409877-73409909 | Rare:8 |