| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71808774-71808823 | Rare:34 | ||||
| chr16:71809001-71809247 | Common:3; Rare:80 | ||||
| chr16:71845879-71846023 | Common:2; Rare:49 | ||||
| chr16:72093565-72093955 | Rare:97 | ||||
| chr16:74296722-74296941 | Rare:93 | ||||
| chr16:74607059-74607132 | Rare:51 | ||||
| chr16:74666828-74667096 | Common:4; Rare:97 | ||||
| chr16:75433291-75433799 | Common:4; Rare:173 | ||||
| chr16:75647615-75647863 | Common:4; Rare:126; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648072-75648280 | Rare:86 | ||||
| chr16:75648631-75648674 | Rare:19 | ||||
| chr16:77191139-77191224 | Common:1; Rare:38 | ||||
| chr16:81006820-81007280 | Common:4; Rare:153 | ||||
| chr16:81314776-81314977 | Common:2; Rare:91 | ||||
| chr16:84116797-84117061 | Common:3; Rare:103 |