| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11915370-11915726 | Common:5; Rare:135 | ||||
| chr16:11915883-11916232 | Common:2; Rare:142 | ||||
| chr16:11976609-11976783 | Common:3; Rare:71 | ||||
| chr16:14071017-14071382 | Common:4; Rare:130 | ||||
| chr16:14186373-14186730 | Common:2; Rare:67 | ||||
| chr16:14630143-14630484 | Rare:139 | ||||
| chr16:14632754-14632995 | Common:1; Rare:78 | ||||
| chr16:14648152-14648490 | Rare:83 | ||||
| chr16:14974729-14975214 | Common:2; Rare:130 | ||||
| chr16:15008488-15008821 | Common:1; Rare:66 | ||||
| chr16:15094193-15094424 | Common:3; Rare:115 | ||||
| chr16:15395908-15396031 | Rare:44 | ||||
| chr16:15643018-15643267 | Rare:75 | ||||
| chr16:15650074-15650293 | Common:1; Rare:112 | ||||
| chr16:15741751-15742109 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):3 |