| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30355183-30355462 | Common:2; Rare:89 | ||||
| chr16:30355707-30355939 | Common:1; Rare:54 | ||||
| chr16:30360513-30360730 | Rare:34 | ||||
| chr16:30526744-30527098 | Common:6; Rare:86 | ||||
| chr16:30534958-30535113 | Common:2; Rare:49 | ||||
| chr16:30535318-30535332 | Rare:1 | ||||
| chr16:30585532-30585936 | Common:1; Rare:92 | ||||
| chr16:30650728-30651021 | Rare:90 | ||||
| chr16:30651382-30651616 | Rare:48 | ||||
| chr16:30658591-30659067 | Common:1; Rare:154 | ||||
| chr16:30659843-30660162 | Rare:101 | ||||
| chr16:30698138-30698298 | Rare:92 | ||||
| chr16:30698347-30698454 | Rare:41 | ||||
| chr16:30698469-30698728 | Common:1; Rare:95 | ||||
| chr16:30698987-30699433 | Rare:117; Clinvar (benign):1 |