| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30651790-30652607 | Rare:312 | ||||
| chr16:30657074-30657800 | Common:7; Rare:219 | ||||
| chr16:30715775-30716211 | Rare:174; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:30721374-30721774 | Rare:104; Clinvar:3 | ||||
| chr16:30775371-30775618 | Common:2; Rare:72 | ||||
| chr16:30775993-30776158 | Rare:34 | ||||
| chr16:30805370-30805700 | Common:2; Rare:145 | ||||
| chr16:30814180-30814680 | Rare:285 | ||||
| chr16:30872287-30872687 | Common:4; Rare:80 | ||||
| chr16:30873408-30873568 | Rare:28 | ||||
| chr16:30874680-30875190 | Common:7; Rare:188 | ||||
| chr16:30875239-30875849 | Common:3; Rare:363 | ||||
| chr16:30876090-30876379 | Common:1; Rare:55 | ||||
| chr16:30876398-30876800 | Common:2; Rare:160 | ||||
| chr16:30876959-30877359 | Common:3; Rare:125 |