| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22436905-22437323 | Rare:142 | ||||
| chr16:22437443-22437585 | Common:1; Rare:45 | ||||
| chr16:22437587-22437921 | Common:4; Rare:83 | ||||
| chr16:23149177-23149287 | Rare:30 | ||||
| chr16:23149353-23149538 | Common:1; Rare:76 | ||||
| chr16:23452667-23452843 | Rare:64; Clinvar (benign):1 | ||||
| chr16:23452965-23452982 | Rare:6 | ||||
| chr16:23453106-23453277 | Rare:54 | ||||
| chr16:23509670-23510019 | Common:6; Rare:81 | ||||
| chr16:23510372-23510842 | Common:5; Rare:167 | ||||
| chr16:23557111-23557262 | Common:1; Rare:54 | ||||
| chr16:23557265-23557850 | Common:4; Rare:226; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:23596222-23596455 | Rare:65 | ||||
| chr16:23640719-23640802 | Common:1; Rare:18 | ||||
| chr16:23641009-23641141 | Rare:43; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 |