| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:163332538-163332673 | Common:1; Rare:18 | ||||
| chr4:163332819-163332882 | Rare:22 | ||||
| chr4:163343794-163343942 | Common:1; Rare:46 | ||||
| chr4:163344534-163344750 | Rare:50 | ||||
| chr4:163494411-163494782 | Common:3; Rare:152 | ||||
| chr4:164956849-164957035 | Common:3; Rare:64 | ||||
| chr4:164977553-164977731 | Rare:47 | ||||
| chr4:165112789-165112990 | Common:1; Rare:66 | ||||
| chr4:165327346-165327776 | Common:3; Rare:132 | ||||
| chr4:165327891-165327939 | Common:1; Rare:12 | ||||
| chr4:165378891-165379083 | Common:2; Rare:47 | ||||
| chr4:167234506-167234811 | Rare:75 | ||||
| chr4:168480452-168480492 | Common:1; Rare:12 | ||||
| chr4:168496728-168497155 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:168631343-168631655 | Common:1; Rare:85 |