| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:52547030-52547500 | Common:2; Rare:115 | ||||
| chr16:53054781-53055067 | Common:2; Rare:63 | ||||
| chr16:53098941-53099341 | Rare:98 | ||||
| chr16:53099620-53100070 | Common:1; Rare:78 | ||||
| chr16:53130800-53131028 | Rare:69 | ||||
| chr16:53131296-53132018 | Common:13; Rare:303 | ||||
| chr16:53207887-53208068 | Common:1; Rare:29 | ||||
| chr16:53208305-53208578 | Rare:51 | ||||
| chr16:53434242-53434877 | Common:4; Rare:303 | ||||
| chr16:53435376-53435776 | Common:2; Rare:107 | ||||
| chr16:53502940-53503101 | Rare:87 | ||||
| chr16:53503130-53503740 | Common:11; Rare:182 | ||||
| chr16:53503767-53504178 | Common:9; Rare:117 | ||||
| chr16:53703809-53704176 | Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:54286200-54286620 | Common:4; Rare:102 |