| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31033456-31033789 | Common:1; Rare:97 | ||||
| chr16:31073726-31073817 | Rare:26 | ||||
| chr16:31074187-31074456 | Common:1; Rare:75 | ||||
| chr16:31108344-31108465 | Rare:34 | ||||
| chr16:31135476-31135843 | Rare:87 | ||||
| chr16:31201822-31202119 | Rare:121 | ||||
| chr16:31202677-31202857 | Common:1; Rare:72 | ||||
| chr16:31442787-31443059 | Common:1; Rare:42 | ||||
| chr16:31458886-31459168 | Rare:83 | ||||
| chr16:31459290-31459517 | Common:1; Rare:94 | ||||
| chr16:31471954-31472186 | Rare:54 | ||||
| chr16:31508365-31508509 | Common:4; Rare:62 | ||||
| chr16:46689136-46689317 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973548-46973796 | Rare:106 | ||||
| chr16:47460904-47461378 | Common:2; Rare:194; Clinvar (benign):2 |