| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22436912-22437133 | Rare:135 | ||||
| chr16:22437120-22437420 | Rare:149 | ||||
| chr16:22437446-22437626 | Common:3; Rare:91 | ||||
| chr16:23148510-23149150 | Common:4; Rare:401 | ||||
| chr16:23149348-23149702 | Common:3; Rare:189 | ||||
| chr16:23452735-23452836 | Rare:41; Clinvar (benign):1 | ||||
| chr16:23453115-23453232 | Rare:72 | ||||
| chr16:23510412-23510568 | Common:5; Rare:84 | ||||
| chr16:23557263-23557830 | Common:7; Rare:391; Clinvar:2; Clinvar (benign):7 | ||||
| chr16:23596229-23596470 | Common:1; Rare:67 | ||||
| chr16:23641212-23641551 | Common:4; Rare:190; Clinvar:2; Clinvar (benign):6 | ||||
| chr16:23678714-23678965 | Common:8; Rare:153 | ||||
| chr16:23694800-23695020 | Rare:96 | ||||
| chr16:24540110-24540680 | Rare:242 | ||||
| chr16:24729604-24729739 | Common:12; Rare:140 |