| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87317374-87317553 | Common:5; Rare:73 | ||||
| chr16:87765901-87766062 | Common:1; Rare:66 | ||||
| chr16:87951280-87951502 | Common:1; Rare:79 | ||||
| chr16:88570159-88570436 | Common:2; Rare:100 | ||||
| chr16:88663070-88663381 | Common:9; Rare:129 | ||||
| chr16:88856891-88857175 | Common:4; Rare:137; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89093765-89093933 | Common:3; Rare:72 | ||||
| chr16:89217619-89217754 | Common:1; Rare:63 | ||||
| chr16:89508312-89508411 | Rare:51 | ||||
| chr16:89560510-89560725 | Rare:99 | ||||
| chr16:89657647-89658130 | Common:3; Rare:245 | ||||
| chr16:89686889-89686952 | Rare:24 | ||||
| chr16:89720865-89721016 | Common:1; Rare:46 | ||||
| chr16:89816613-89816754 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89873442-89873715 | Common:4; Rare:124 |