| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2777245-2777366 | Common:1; Rare:46 | ||||
| chr16:3134824-3135137 | Common:3; Rare:83 | ||||
| chr16:3283305-3283560 | Common:4; Rare:72 | ||||
| chr16:3305243-3305534 | Common:4; Rare:90 | ||||
| chr16:3400967-3401254 | Common:6; Rare:106 | ||||
| chr16:3443450-3443729 | Common:3; Rare:93 | ||||
| chr16:4263730-4263849 | Common:1; Rare:39 | ||||
| chr16:4425737-4425883 | Common:1; Rare:67 | ||||
| chr16:4680058-4680230 | Common:2; Rare:74 | ||||
| chr16:4734176-4734537 | Common:1; Rare:119 | ||||
| chr16:4847258-4847442 | Common:1; Rare:79 | ||||
| chr16:5033920-5033960 | Rare:16 | ||||
| chr16:8797610-8797925 | Common:1; Rare:128; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:11797136-11797545 | Common:4; Rare:155 | ||||
| chr16:11976623-11976763 | Common:2; Rare:50 |