| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69408520-69408810 | Common:4; Rare:83 | ||||
| chr16:69424316-69424976 | Common:9; Rare:308 | ||||
| chr16:69565681-69566173 | Common:9; Rare:309 | ||||
| chr16:69726355-69727099 | Common:11; Rare:361 | ||||
| chr16:69762236-69762385 | Common:2; Rare:76 | ||||
| chr16:70114088-70114413 | Common:4; Rare:153 | ||||
| chr16:70251857-70251993 | Rare:71 | ||||
| chr16:70289395-70289822 | Common:3; Rare:250; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:70299068-70299295 | Common:1; Rare:85 | ||||
| chr16:70346735-70346987 | Common:4; Rare:228 | ||||
| chr16:70438984-70439103 | Rare:53 | ||||
| chr16:70439010-70439457 | Common:2; Rare:150 | ||||
| chr16:70454312-70454639 | Common:4; Rare:168 | ||||
| chr16:70523063-70523463 | Common:5; Rare:135; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:70523451-70523899 | Common:6; Rare:286; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 |