| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86555179-86555306 | Rare:65 | ||||
| chr16:87317370-87317508 | Common:4; Rare:52 | ||||
| chr16:87383581-87383982 | Common:2; Rare:149; Clinvar (benign):1 | ||||
| chr16:87765901-87766035 | Rare:54 | ||||
| chr16:88570174-88570467 | Common:1; Rare:111 | ||||
| chr16:88663070-88663371 | Common:8; Rare:124 | ||||
| chr16:88706203-88706527 | Common:4; Rare:141 | ||||
| chr16:88856932-88857161 | Common:4; Rare:103; Clinvar (benign):2 | ||||
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89508289-89508455 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560535-89560725 | Rare:84 | ||||
| chr16:89657644-89658138 | Common:3; Rare:247 | ||||
| chr16:89720865-89721021 | Common:1; Rare:47 | ||||
| chr16:89873490-89873789 | Common:2; Rare:137 | ||||
| chr16:89923139-89923348 | Rare:81 |