| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31033099-31033693 | Common:13; Rare:804 | ||||
| chr16:31034190-31034520 | Rare:137 | ||||
| chr16:31072410-31072829 | Rare:149 | ||||
| chr16:31072784-31074100 | Common:15; Rare:1093 | ||||
| chr16:31074109-31074509 | Common:12; Rare:585 | ||||
| chr16:31093305-31094161 | Common:6; Rare:216; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:31094065-31095251 | Common:5; Rare:869; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):8 | ||||
| chr16:31105600-31106100 | Common:16; Rare:249 | ||||
| chr16:31108140-31108540 | Common:2; Rare:301 | ||||
| chr16:31117252-31118154 | Common:16; Rare:707 | ||||
| chr16:31134936-31135336 | Common:1; Rare:105 | ||||
| chr16:31135564-31135964 | Common:1; Rare:166 | ||||
| chr16:31142138-31142538 | Common:9; Rare:289 | ||||
| chr16:31179732-31180920 | Common:28; Rare:1573; Clinvar:8; Clinvar (benign):8 | ||||
| chr16:31201821-31202987 | Common:11; Rare:1186 |