| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89721384-89721614 | Common:3; Rare:110 | ||||
| chr16:89764448-89764805 | Rare:114 | ||||
| chr16:89764906-89765245 | Common:4; Rare:147; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr16:89816554-89817057 | Common:8; Rare:264; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89863820-89864294 | Common:4; Rare:118 | ||||
| chr16:89873289-89873728 | Common:5; Rare:185 | ||||
| chr16:89873799-89873900 | Common:4; Rare:36 | ||||
| chr16:89874027-89874469 | Common:5; Rare:126 | ||||
| chr16:89917993-89918189 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:89923167-89923369 | Rare:84 | ||||
| chr16:89948091-89948343 | Common:8; Rare:77 | ||||
| chr16:89972426-89972695 | Common:1; Rare:99 | ||||
| chr16:89972733-89972972 | Common:3; Rare:92 | ||||
| chr16:90008958-90009119 | Common:3; Rare:37 | ||||
| chr16:90022492-90022694 | Common:1; Rare:75 |