| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74666848-74667169 | Common:4; Rare:106 | ||||
| chr16:75433379-75433787 | Common:4; Rare:130 | ||||
| chr16:75647614-75647794 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:81006839-81007272 | Common:3; Rare:144 | ||||
| chr16:82170179-82170333 | Common:3; Rare:81 | ||||
| chr16:84116806-84117057 | Common:3; Rare:96 | ||||
| chr16:84699814-84700035 | Common:2; Rare:93 | ||||
| chr16:85799302-85799757 | Common:3; Rare:143 | ||||
| chr16:86555180-86555283 | Rare:53 | ||||
| chr16:88570170-88570441 | Common:2; Rare:100 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:89217632-89217723 | Common:1; Rare:39 | ||||
| chr16:89560537-89560717 | Rare:75 | ||||
| chr16:89657669-89657846 | Rare:90 | ||||
| chr17:1516605-1516960 | Common:1; Rare:125 |