| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31117898-31118059 | Rare:41 | ||||
| chr16:31202644-31202784 | Rare:58 | ||||
| chr16:31442766-31443061 | Common:1; Rare:47 | ||||
| chr16:31458441-31458684 | Common:2; Rare:68 | ||||
| chr16:31459091-31459161 | Rare:23 | ||||
| chr16:31459288-31459527 | Common:1; Rare:101 | ||||
| chr16:31472109-31472186 | Rare:21 | ||||
| chr16:31508351-31508508 | Common:4; Rare:69 | ||||
| chr16:46689130-46689313 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689706 | Common:2; Rare:82; Clinvar (benign):2 | ||||
| chr16:46973519-46973781 | Rare:101 | ||||
| chr16:47461027-47461388 | Common:2; Rare:142; Clinvar (benign):2 | ||||
| chr16:48244254-48244516 | Common:2; Rare:80 | ||||
| chr16:48365873-48366126 | Common:5; Rare:73 | ||||
| chr16:48610195-48610311 | Common:2; Rare:49 |