| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29899187-29899308 | Common:1; Rare:21 | ||||
| chr16:29961942-29962165 | Common:1; Rare:73 | ||||
| chr16:29973611-29973932 | Common:5; Rare:109 | ||||
| chr16:29995601-29995713 | Rare:50 | ||||
| chr16:29996061-29996302 | Common:2; Rare:85 | ||||
| chr16:30010954-30011186 | Rare:59 | ||||
| chr16:30021288-30021422 | Rare:23 | ||||
| chr16:30030785-30030889 | Rare:15 | ||||
| chr16:30064326-30064497 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr16:30065525-30065841 | Rare:113 | ||||
| chr16:30075875-30076055 | Rare:60 | ||||
| chr16:30091878-30092119 | Common:1; Rare:54 | ||||
| chr16:30096158-30096507 | Common:1; Rare:100 | ||||
| chr16:30123058-30123389 | Common:6; Rare:98 | ||||
| chr16:30183492-30183634 | Common:2; Rare:37 |