| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19691265-19691304 | Rare:6 | ||||
| chr16:19862043-19862146 | Rare:20 | ||||
| chr16:20674728-20674771 | Common:1; Rare:10 | ||||
| chr16:20676146-20676272 | Common:2; Rare:23 | ||||
| chr16:20763904-20764029 | Common:2; Rare:17 | ||||
| chr16:20806331-20806617 | Rare:95 | ||||
| chr16:20900226-20900850 | Common:4; Rare:147 | ||||
| chr16:21652595-21652782 | Rare:41 | ||||
| chr16:21953038-21953414 | Common:1; Rare:96; Clinvar (benign):3 | ||||
| chr16:22206217-22206345 | Rare:45 | ||||
| chr16:22436987-22437067 | Rare:28 | ||||
| chr16:22437166-22437318 | Rare:46 | ||||
| chr16:22437435-22437490 | Rare:15 | ||||
| chr16:22437505-22437671 | Common:2; Rare:42 | ||||
| chr16:23557304-23557557 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):2 |