| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74304201-74304381 | Common:2; Rare:41 | ||||
| chr16:74607074-74607231 | Rare:83 | ||||
| chr16:74701076-74701293 | Common:2; Rare:40 | ||||
| chr16:75248144-75248304 | Rare:44 | ||||
| chr16:75306405-75306648 | Rare:33 | ||||
| chr16:75433379-75433812 | Common:4; Rare:136 | ||||
| chr16:75464372-75464449 | Common:2; Rare:33 | ||||
| chr16:75566283-75566447 | Rare:90 | ||||
| chr16:75635786-75635999 | Rare:71; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:75647614-75647864 | Common:4; Rare:126; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190702-77191010 | Common:10; Rare:101 | ||||
| chr16:77191085-77191246 | Common:2; Rare:66 | ||||
| chr16:79600684-79600958 | Common:1; Rare:79 | ||||
| chr16:80540807-80541025 | Common:4; Rare:88 | ||||
| chr16:81006337-81006586 | Common:2; Rare:68 |