| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89657644-89658120 | Common:3; Rare:245 | ||||
| chr16:89686631-89686704 | Common:5; Rare:46 | ||||
| chr16:89873463-89873715 | Common:2; Rare:112 | ||||
| chr16:89883225-89883423 | Rare:82 | ||||
| chr16:89948560-89948803 | Common:3; Rare:72 | ||||
| chr16:89972485-89972658 | Common:1; Rare:64 | ||||
| chr16:90022551-90022713 | Rare:65 | ||||
| chr17:714777-714946 | Common:2; Rare:55 | ||||
| chr17:752152-752354 | Common:2; Rare:81 | ||||
| chr17:996787-997159 | Common:2; Rare:111 | ||||
| chr17:1400046-1400431 | Common:3; Rare:152 | ||||
| chr17:1485720-1486065 | Common:4; Rare:116 | ||||
| chr17:1516588-1516969 | Common:2; Rare:133 | ||||
| chr17:1684794-1685067 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716191-1716536 | Common:3; Rare:106 |