| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85799116-85799196 | Common:1; Rare:28 | ||||
| chr16:85799353-85799752 | Common:3; Rare:119 | ||||
| chr16:86555172-86555312 | Rare:70 | ||||
| chr16:87317384-87317529 | Common:3; Rare:56 | ||||
| chr16:87765919-87766068 | Common:1; Rare:61 | ||||
| chr16:88570174-88570489 | Common:1; Rare:121 | ||||
| chr16:88650955-88651198 | Common:1; Rare:85; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88663068-88663382 | Common:9; Rare:130 | ||||
| chr16:88706248-88706522 | Common:4; Rare:126 | ||||
| chr16:88856878-88857161 | Common:4; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217619-89217721 | Common:1; Rare:46 | ||||
| chr16:89560526-89560725 | Rare:89 | ||||
| chr16:89657644-89658091 | Common:3; Rare:235 | ||||
| chr16:89686596-89686704 | Common:6; Rare:53 | ||||
| chr16:89720869-89721130 | Common:3; Rare:78 |