| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69726435-69726861 | Common:4; Rare:114 | ||||
| chr16:69754843-69755228 | Common:1; Rare:124 | ||||
| chr16:70114208-70114621 | Common:3; Rare:135 | ||||
| chr16:70251892-70252028 | Common:1; Rare:60 | ||||
| chr16:70252057-70252330 | Common:1; Rare:58 | ||||
| chr16:70289405-70289580 | Rare:71; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:70346751-70346975 | Common:2; Rare:112 | ||||
| chr16:70454324-70454619 | Common:2; Rare:76 | ||||
| chr16:70523391-70523925 | Common:3; Rare:190; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70549821-70550004 | Rare:40 | ||||
| chr16:71764356-71764712 | Rare:82 | ||||
| chr16:71808367-71808474 | Rare:39 | ||||
| chr16:71808752-71808930 | Common:1; Rare:83 | ||||
| chr16:71808970-71809251 | Common:3; Rare:101 | ||||
| chr16:71845905-71846017 | Common:1; Rare:35 |