| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46973606-46973761 | Rare:71 | ||||
| chr16:47461041-47461343 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr16:53054819-53055048 | Common:2; Rare:56 | ||||
| chr16:53099002-53099189 | Rare:41 | ||||
| chr16:53703809-53704206 | Common:1; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56451309-56451605 | Common:1; Rare:96 | ||||
| chr16:56608429-56608694 | Common:2; Rare:81 | ||||
| chr16:56638504-56638684 | Common:1; Rare:72 | ||||
| chr16:56729812-56730189 | Common:2; Rare:85 | ||||
| chr16:56931862-56932166 | Common:3; Rare:134 | ||||
| chr16:57185990-57186335 | Common:1; Rare:99 | ||||
| chr16:57244974-57245328 | Common:3; Rare:115 | ||||
| chr16:57447360-57447503 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58001318-58001436 | Rare:31 | ||||
| chr16:58129274-58129523 | Common:2; Rare:78 |