| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75566216-75566512 | Common:3; Rare:143 | ||||
| chr16:75623218-75623390 | Common:3; Rare:64 | ||||
| chr16:75647601-75647863 | Common:4; Rare:131; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648068-75648510 | Rare:165 | ||||
| chr16:75648633-75648733 | Rare:38 | ||||
| chr16:77190686-77191042 | Common:10; Rare:114 | ||||
| chr16:77191065-77191321 | Common:2; Rare:96 | ||||
| chr16:77211920-77212114 | Common:3; Rare:44 | ||||
| chr16:78099586-78099731 | Common:1; Rare:68 | ||||
| chr16:79599771-79599886 | Rare:26 | ||||
| chr16:79599964-79600367 | Common:5; Rare:125 | ||||
| chr16:79600710-79600975 | Common:1; Rare:72 | ||||
| chr16:80540916-80541025 | Common:2; Rare:39 | ||||
| chr16:81006430-81006558 | Rare:37 | ||||
| chr16:81006825-81007264 | Common:3; Rare:148 |