| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31094544-31094885 | Common:2; Rare:215; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:31108275-31108486 | Rare:89 | ||||
| chr16:31117876-31118078 | Rare:93 | ||||
| chr16:31141982-31142822 | Common:8; Rare:283 | ||||
| chr16:31149710-31149920 | Rare:72 | ||||
| chr16:31150164-31150475 | Common:1; Rare:61 | ||||
| chr16:31179774-31180238 | Common:4; Rare:351; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180583-31180867 | Common:6; Rare:199 | ||||
| chr16:31457870-31458320 | Common:1; Rare:135 | ||||
| chr16:31458611-31458864 | Common:2; Rare:75 | ||||
| chr16:31458985-31459161 | Rare:76 | ||||
| chr16:31459226-31459517 | Common:2; Rare:219 | ||||
| chr16:31471924-31472186 | Rare:87 | ||||
| chr16:31508328-31508535 | Common:8; Rare:163 | ||||
| chr16:31713151-31713306 | Rare:33 |