| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158723338-158723608 | Common:2; Rare:98 | ||||
| chr4:174283668-174283904 | Common:1; Rare:41 | ||||
| chr4:184649440-184649746 | Common:4; Rare:98 | ||||
| chr5:218140-218340 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:1799795-1799971 | Common:4; Rare:87 | ||||
| chr5:7869010-7869200 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr5:31532069-31532315 | Common:1; Rare:65 | ||||
| chr5:33440634-33441011 | Common:3; Rare:94 | ||||
| chr5:33891982-33892303 | Rare:76 | ||||
| chr5:34915493-34915741 | Common:1; Rare:56 | ||||
| chr5:36151881-36152120 | Rare:66 | ||||
| chr5:39424945-39425291 | Common:3; Rare:71 | ||||
| chr5:40679660-40679938 | Common:2; Rare:67 | ||||
| chr5:43483842-43483913 | Common:1; Rare:29 | ||||
| chr5:43603105-43603260 | Rare:36 |