| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89491563-89491963 | Common:2; Rare:143 | ||||
| chr16:89506877-89507803 | Common:7; Rare:443 | ||||
| chr16:89507801-89507903 | Rare:36 | ||||
| chr16:89507816-89508564 | Common:14; Rare:910; Clinvar:16; Clinvar (benign):12; Clinvar (pathogenic):6 | ||||
| chr16:89508875-89509275 | Common:2; Rare:142 | ||||
| chr16:89560280-89560786 | Common:4; Rare:938 | ||||
| chr16:89561206-89561606 | Common:1; Rare:178 | ||||
| chr16:89562274-89562899 | Common:23; Rare:462 | ||||
| chr16:89574880-89575280 | Common:3; Rare:105 | ||||
| chr16:89575183-89575956 | Common:16; Rare:524 | ||||
| chr16:89587030-89587330 | Common:20; Rare:136 | ||||
| chr16:89646130-89647080 | Common:11; Rare:441; Clinvar (benign):4 | ||||
| chr16:89657480-89658794 | Common:33; Rare:1990; Clinvar (benign):7 | ||||
| chr16:89686526-89686772 | Common:18; Rare:224 | ||||
| chr16:89686688-89687329 | Common:23; Rare:700 |