| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074187-31074444 | Common:1; Rare:71 | ||||
| chr16:31094725-31094817 | Rare:33 | ||||
| chr16:31202656-31202980 | Common:2; Rare:114 | ||||
| chr16:31442763-31443059 | Common:1; Rare:48 | ||||
| chr16:31459297-31459517 | Common:1; Rare:89 | ||||
| chr16:31472109-31472189 | Rare:22 | ||||
| chr16:31508389-31508509 | Common:4; Rare:49 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689503-46689714 | Common:2; Rare:87; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973626-46973768 | Rare:67 | ||||
| chr16:47461012-47461388 | Common:2; Rare:151; Clinvar (benign):2 | ||||
| chr16:50693498-50693612 | Rare:44 | ||||
| chr16:50741723-50742121 | Common:7; Rare:117; Clinvar:1 | ||||
| chr16:53703817-53704215 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286711-54286964 | Common:1; Rare:73 |