| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:24729920-24730240 | Common:2; Rare:153 | ||||
| chr16:25015249-25015467 | Common:4; Rare:136 | ||||
| chr16:25111475-25111856 | Common:3; Rare:203 | ||||
| chr16:25257428-25257614 | Rare:134 | ||||
| chr16:25257797-25258107 | Common:13; Rare:241 | ||||
| chr16:25258172-25258420 | Common:9; Rare:173 | ||||
| chr16:27203409-27203578 | Rare:107 | ||||
| chr16:27203590-27204062 | Common:8; Rare:276 | ||||
| chr16:27268671-27268912 | Common:2; Rare:156 | ||||
| chr16:27313786-27314013 | Common:4; Rare:113 | ||||
| chr16:27470550-27471140 | Common:1; Rare:188 | ||||
| chr16:27549843-27550180 | Common:4; Rare:258 | ||||
| chr16:28211775-28212305 | Common:8; Rare:318 | ||||
| chr16:28491752-28492578 | Common:7; Rare:268; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr16:28538908-28539223 | Common:3; Rare:101 |