| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58517076-58518933 | Common:13; Rare:763 | ||||
| chr16:58599310-58599710 | Common:2; Rare:72 | ||||
| chr16:58629341-58629741 | Common:3; Rare:92 | ||||
| chr16:58629742-58630250 | Common:19; Rare:841 | ||||
| chr16:58630243-58630667 | Common:3; Rare:236 | ||||
| chr16:58684590-58684990 | Common:5; Rare:248 | ||||
| chr16:58734111-58734524 | Common:17; Rare:332 | ||||
| chr16:66516590-66517159 | Common:2; Rare:315; Clinvar (pathogenic):1 | ||||
| chr16:66524779-66525179 | Common:4; Rare:75 | ||||
| chr16:66549650-66550210 | Common:22; Rare:610; Clinvar:2; Clinvar (benign):12; Clinvar (pathogenic):5 | ||||
| chr16:66550146-66550490 | Rare:135; Clinvar:2 | ||||
| chr16:66551190-66551900 | Common:8; Rare:280 | ||||
| chr16:66552414-66552926 | Common:1; Rare:666 | ||||
| chr16:66553192-66553592 | Common:1; Rare:71 | ||||
| chr16:66603667-66604067 | Common:4; Rare:83 |