| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89686668-89686782 | Common:5; Rare:73 | ||||
| chr16:89686830-89686943 | Common:1; Rare:45 | ||||
| chr16:89686895-89687842 | Common:8; Rare:473 | ||||
| chr16:89701599-89701867 | Common:3; Rare:252 | ||||
| chr16:89701926-89702340 | Common:27; Rare:303 | ||||
| chr16:89711501-89712018 | Common:7; Rare:315 | ||||
| chr16:89712108-89712782 | Common:7; Rare:391 | ||||
| chr16:89718454-89719437 | Common:16; Rare:437 | ||||
| chr16:89720610-89721230 | Common:11; Rare:473 | ||||
| chr16:89721237-89721719 | Common:9; Rare:423 | ||||
| chr16:89721845-89721983 | Rare:87 | ||||
| chr16:89722070-89722270 | Rare:63 | ||||
| chr16:89722300-89723217 | Common:12; Rare:754 | ||||
| chr16:89816479-89816891 | Common:20; Rare:523; Clinvar:16; Clinvar (benign):11; Clinvar (pathogenic):11 | ||||
| chr16:89828196-89828588 | Common:7; Rare:376 |