| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74701131-74701343 | Common:1; Rare:47 | ||||
| chr16:75433408-75433765 | Common:3; Rare:106 | ||||
| chr16:75623232-75623552 | Common:3; Rare:106 | ||||
| chr16:75647614-75647776 | Common:1; Rare:86; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:78099645-78099727 | Rare:42 | ||||
| chr16:81006839-81007272 | Common:3; Rare:144 | ||||
| chr16:82170168-82170382 | Common:4; Rare:111 | ||||
| chr16:84116806-84117054 | Common:3; Rare:95 | ||||
| chr16:84504616-84504870 | Common:9; Rare:112 | ||||
| chr16:84699850-84700020 | Common:2; Rare:75 | ||||
| chr16:85027618-85027801 | Common:1; Rare:95 | ||||
| chr16:85613055-85613328 | Common:1; Rare:100 | ||||
| chr16:85799312-85799752 | Common:3; Rare:136 | ||||
| chr16:86555185-86555312 | Rare:61 | ||||
| chr16:87317402-87317527 | Common:2; Rare:46 |