| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:17013894-17014294 | Common:6; Rare:124 | ||||
| chr16:17023145-17023894 | Common:5; Rare:286 | ||||
| chr16:17025449-17025763 | Common:1; Rare:72 | ||||
| chr16:17026867-17027078 | Common:4; Rare:70 | ||||
| chr16:17027821-17027933 | Common:1; Rare:15 | ||||
| chr16:17068500-17068890 | Rare:117 | ||||
| chr16:17070908-17071236 | Common:1; Rare:118 | ||||
| chr16:17076347-17076747 | Common:4; Rare:132 | ||||
| chr16:17134580-17134980 | Common:1; Rare:181; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr16:17239300-17239600 | Common:7; Rare:44 | ||||
| chr16:17278935-17279335 | Common:4; Rare:77 | ||||
| chr16:17282230-17282600 | Common:6; Rare:111 | ||||
| chr16:17301861-17302116 | Common:1; Rare:50 | ||||
| chr16:17305773-17306090 | Common:2; Rare:90 | ||||
| chr16:17343128-17343318 | Common:1; Rare:34 |