| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132495-69132673 | Rare:65 | ||||
| chr16:69339532-69339824 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69726536-69726727 | Common:3; Rare:42 | ||||
| chr16:70523462-70523852 | Common:3; Rare:145; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:72093572-72093934 | Rare:90 | ||||
| chr16:74666850-74667058 | Common:1; Rare:78 | ||||
| chr16:75433461-75433804 | Common:4; Rare:97 | ||||
| chr16:75647636-75647863 | Common:4; Rare:110; Clinvar:3 | ||||
| chr16:77191145-77191213 | Common:1; Rare:31 | ||||
| chr16:81006803-81007282 | Common:4; Rare:162 | ||||
| chr16:82170153-82170337 | Common:4; Rare:100 | ||||
| chr16:84116791-84117066 | Common:3; Rare:110 | ||||
| chr16:84504592-84504876 | Common:9; Rare:125 | ||||
| chr16:85027594-85027778 | Common:1; Rare:98 | ||||
| chr16:85799513-85799729 | Common:2; Rare:64 |