| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85027578-85027828 | Common:2; Rare:139 | ||||
| chr16:85799116-85799197 | Common:1; Rare:28 | ||||
| chr16:85799291-85799752 | Common:3; Rare:147 | ||||
| chr16:86555180-86555306 | Rare:64 | ||||
| chr16:87317394-87317516 | Common:2; Rare:45 | ||||
| chr16:87765919-87766044 | Rare:48 | ||||
| chr16:88570167-88570463 | Common:2; Rare:112 | ||||
| chr16:88663070-88663389 | Common:9; Rare:135 | ||||
| chr16:88706251-88706546 | Common:4; Rare:140 | ||||
| chr16:88856932-88857183 | Common:4; Rare:117; Clinvar (benign):2 | ||||
| chr16:89217602-89217749 | Common:1; Rare:72 | ||||
| chr16:89508312-89508424 | Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560515-89560717 | Rare:87 | ||||
| chr16:89657644-89658047 | Common:3; Rare:211 | ||||
| chr16:89686567-89686704 | Common:6; Rare:61 |