| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46790279-46790679 | Common:1; Rare:78 | ||||
| chr16:46830060-46830590 | Common:2; Rare:147 | ||||
| chr16:46830612-46831012 | Common:1; Rare:105 | ||||
| chr16:46831087-46831763 | Common:10; Rare:595 | ||||
| chr16:46883897-46884839 | Common:15; Rare:708; Clinvar (pathogenic):1 | ||||
| chr16:46915300-46915780 | Common:6; Rare:120 | ||||
| chr16:46972719-46973119 | Common:3; Rare:203 | ||||
| chr16:46973076-46973476 | Common:1; Rare:151 | ||||
| chr16:46973514-46973914 | Rare:702 | ||||
| chr16:47142885-47143660 | Common:2; Rare:341 | ||||
| chr16:47143832-47144232 | Rare:466 | ||||
| chr16:47144365-47144765 | Rare:91 | ||||
| chr16:47458323-47458723 | Rare:60 | ||||
| chr16:47460903-47461467 | Common:18; Rare:1124; Clinvar:1; Clinvar (benign):16 | ||||
| chr16:47461660-47462380 | Common:4; Rare:404 |