| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84504612-84504861 | Common:8; Rare:109 | ||||
| chr16:85027620-85027819 | Common:1; Rare:106 | ||||
| chr16:85799520-85799748 | Common:2; Rare:66 | ||||
| chr16:87765908-87766028 | Rare:48 | ||||
| chr16:88570174-88570441 | Common:1; Rare:98 | ||||
| chr16:88663076-88663362 | Common:7; Rare:116 | ||||
| chr16:88706203-88706527 | Common:4; Rare:141 | ||||
| chr16:88856925-88857148 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217625-89217738 | Common:1; Rare:50 | ||||
| chr16:89508296-89508420 | Rare:69; Clinvar (pathogenic):1 | ||||
| chr16:89560555-89560725 | Rare:75 | ||||
| chr16:89657637-89658089 | Common:3; Rare:237 | ||||
| chr16:89686576-89686704 | Common:6; Rare:59 | ||||
| chr16:89816640-89816735 | Common:1; Rare:38; Clinvar:1 | ||||
| chr16:89873428-89873820 | Common:5; Rare:185 |