| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75265828-75266031 | Common:3; Rare:81 | ||||
| chr16:75305334-75305737 | Common:2; Rare:70 | ||||
| chr16:75433263-75433398 | Rare:65 | ||||
| chr16:75433450-75433539 | Common:1; Rare:30 | ||||
| chr16:75556218-75556355 | Common:1; Rare:48; Clinvar (benign):3 | ||||
| chr16:75566216-75566443 | Common:2; Rare:114 | ||||
| chr16:75623180-75623432 | Common:4; Rare:98 | ||||
| chr16:75647576-75647904 | Common:4; Rare:158; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648084-75648290 | Rare:84 | ||||
| chr16:75648439-75648488 | Rare:15 | ||||
| chr16:75648614-75648850 | Rare:73 | ||||
| chr16:77190680-77191218 | Common:14; Rare:184 | ||||
| chr16:77212172-77212368 | Common:4; Rare:85 | ||||
| chr16:81006436-81006549 | Rare:32 | ||||
| chr16:81006789-81007280 | Common:5; Rare:165 |