| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85613091-85613221 | Common:1; Rare:51 | ||||
| chr16:85799557-85799752 | Common:2; Rare:56 | ||||
| chr16:85899011-85899185 | Common:3; Rare:47 | ||||
| chr16:86555164-86555308 | Rare:72 | ||||
| chr16:87317370-87317516 | Common:4; Rare:54 | ||||
| chr16:87765919-87766044 | Rare:48 | ||||
| chr16:88570174-88570524 | Common:1; Rare:129 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88706170-88706548 | Common:4; Rare:166 | ||||
| chr16:88856937-88857188 | Common:4; Rare:120; Clinvar (benign):2 | ||||
| chr16:89217607-89217738 | Common:1; Rare:64 | ||||
| chr16:89508305-89508424 | Rare:62; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560535-89560725 | Rare:84 | ||||
| chr16:89657637-89657847 | Common:1; Rare:105 | ||||
| chr16:89686567-89686712 | Common:6; Rare:68 |