| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70114275-70114362 | Common:1; Rare:25 | ||||
| chr16:70289423-70289678 | Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70346744-70346950 | Common:1; Rare:100 | ||||
| chr16:70454521-70454614 | Common:1; Rare:29 | ||||
| chr16:70523451-70523903 | Common:3; Rare:163; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71723854-71724166 | Common:6; Rare:102 | ||||
| chr16:71808778-71808830 | Rare:38 | ||||
| chr16:71808832-71808916 | Common:1; Rare:34 | ||||
| chr16:71809006-71809250 | Common:3; Rare:82 | ||||
| chr16:71894362-71894460 | Rare:30 | ||||
| chr16:71895254-71895588 | Common:3; Rare:127 | ||||
| chr16:72008593-72008784 | Common:3; Rare:67; Clinvar (benign):2 | ||||
| chr16:72093471-72093944 | Rare:122 | ||||
| chr16:72094369-72094414 | Common:1; Rare:6 | ||||
| chr16:73059067-73059139 | Rare:10 |