| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28925170-28925266 | Rare:25 | ||||
| chr16:28974647-28974792 | Common:1; Rare:60 | ||||
| chr16:29790504-29790804 | Common:1; Rare:117; Clinvar (benign):2 | ||||
| chr16:29805482-29805624 | Common:1; Rare:64 | ||||
| chr16:29807779-29808138 | Common:2; Rare:201 | ||||
| chr16:29899169-29899538 | Common:2; Rare:66 | ||||
| chr16:29900551-29900676 | Common:1; Rare:21 | ||||
| chr16:29926220-29926321 | Common:2; Rare:34 | ||||
| chr16:29961950-29962141 | Common:1; Rare:59 | ||||
| chr16:29995573-29995707 | Common:1; Rare:64 | ||||
| chr16:29996073-29996296 | Common:2; Rare:78 | ||||
| chr16:30030795-30030965 | Rare:22 | ||||
| chr16:30053019-30053167 | Common:1; Rare:55 | ||||
| chr16:30064093-30064497 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr16:30065566-30065889 | Rare:108 |