| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19067811-19068025 | Common:2; Rare:53 | ||||
| chr16:19113701-19113983 | Common:1; Rare:53 | ||||
| chr16:19523827-19523966 | Common:2; Rare:21 | ||||
| chr16:19884805-19885134 | Common:2; Rare:96 | ||||
| chr16:20741704-20741847 | Common:1; Rare:65 | ||||
| chr16:20806338-20806617 | Rare:93 | ||||
| chr16:20868953-20869034 | Common:1; Rare:14 | ||||
| chr16:20899729-20899908 | Rare:34 | ||||
| chr16:20900019-20900926 | Common:6; Rare:208 | ||||
| chr16:20900964-20901108 | Common:1; Rare:30 | ||||
| chr16:21158524-21158718 | Common:1; Rare:57 | ||||
| chr16:21652572-21652824 | Rare:60 | ||||
| chr16:21952979-21953419 | Common:1; Rare:110; Clinvar (benign):3 | ||||
| chr16:21957244-21957566 | Rare:108; Clinvar (benign):1 | ||||
| chr16:22206049-22206363 | Common:1; Rare:87 |