| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4476273-4476467 | Common:3; Rare:73 | ||||
| chr16:4538427-4538596 | Common:1; Rare:60 | ||||
| chr16:4538756-4538919 | Rare:64 | ||||
| chr16:4614853-4615096 | Common:1; Rare:73 | ||||
| chr16:4693453-4693729 | Common:2; Rare:117 | ||||
| chr16:4734231-4734534 | Rare:95 | ||||
| chr16:4767126-4767447 | Common:2; Rare:96 | ||||
| chr16:4847252-4847417 | Common:1; Rare:74 | ||||
| chr16:5033926-5033955 | Rare:8 | ||||
| chr16:5071791-5071849 | Rare:28; Clinvar (benign):1 | ||||
| chr16:8621620-8621703 | Common:1; Rare:33 | ||||
| chr16:8797610-8797877 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:10580581-10580855 | Common:2; Rare:93 | ||||
| chr16:10743746-10743872 | Rare:48 | ||||
| chr16:11345251-11345451 | Common:1; Rare:70 |