| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30065575-30065921 | Rare:117 | ||||
| chr16:30069297-30069673 | Common:1; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:30069720-30069943 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:30075878-30076060 | Common:1; Rare:60 | ||||
| chr16:30096974-30097094 | Rare:19 | ||||
| chr16:30123118-30123334 | Common:4; Rare:62 | ||||
| chr16:30355210-30355453 | Common:2; Rare:84 | ||||
| chr16:30407435-30407645 | Rare:73 | ||||
| chr16:30445871-30446049 | Common:1; Rare:42 | ||||
| chr16:30534743-30535102 | Common:3; Rare:109 | ||||
| chr16:30698458-30698644 | Common:1; Rare:72 | ||||
| chr16:30748128-30748447 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762080-30762335 | Common:3; Rare:89 | ||||
| chr16:30923242-30923592 | Common:1; Rare:87 | ||||
| chr16:31073701-31073848 | Rare:47 |