| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89948672-89948806 | Common:2; Rare:35 | ||||
| chr16:89972478-89972627 | Common:1; Rare:55 | ||||
| chr16:90022529-90022703 | Rare:67 | ||||
| chr17:714782-714915 | Common:2; Rare:45 | ||||
| chr17:752152-752598 | Common:3; Rare:162 | ||||
| chr17:996784-997197 | Common:2; Rare:138 | ||||
| chr17:1078967-1079008 | Rare:16 | ||||
| chr17:1400046-1400332 | Common:2; Rare:117 | ||||
| chr17:1516674-1516977 | Common:1; Rare:111 | ||||
| chr17:1684802-1685030 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:1716204-1716523 | Common:3; Rare:96 | ||||
| chr17:1829812-1830082 | Common:7; Rare:114 | ||||
| chr17:2214311-2214463 | Common:1; Rare:30 | ||||
| chr17:2303728-2303980 | Common:2; Rare:96 | ||||
| chr17:2336398-2336548 | Rare:68 |