| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30893966-30894252 | Common:5; Rare:74 | ||||
| chr16:30923227-30923600 | Common:1; Rare:89 | ||||
| chr16:31033273-31033597 | Common:2; Rare:103 | ||||
| chr16:31073701-31073837 | Rare:44 | ||||
| chr16:31074182-31074451 | Common:2; Rare:73 | ||||
| chr16:31108343-31108488 | Rare:38 | ||||
| chr16:31459309-31459510 | Common:1; Rare:83 | ||||
| chr16:31472109-31472427 | Common:1; Rare:70 | ||||
| chr16:31508374-31508454 | Rare:32 | ||||
| chr16:46689134-46689297 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973581-46973849 | Rare:117 | ||||
| chr16:47461038-47461365 | Common:2; Rare:120; Clinvar (benign):2 | ||||
| chr16:53054829-53055048 | Common:2; Rare:54 | ||||
| chr16:53099087-53099190 | Rare:21 | ||||
| chr16:53703821-53704192 | Rare:110; Clinvar:4; Clinvar (benign):1 |