| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113747387-113748118 | Common:1; Rare:125 | ||||
| chr3:113947510-113948144 | Common:7; Rare:337 | ||||
| chr3:114056010-114056420 | Common:7; Rare:177 | ||||
| chr3:114056440-114056998 | Common:14; Rare:945 | ||||
| chr3:115146800-115148082 | Common:33; Rare:1123 | ||||
| chr3:119034690-119035242 | Common:9; Rare:385 | ||||
| chr3:119240168-119240664 | Common:11; Rare:269 | ||||
| chr3:119240610-119240760 | Common:1; Rare:67 | ||||
| chr3:119240797-119241197 | Common:4; Rare:259 | ||||
| chr3:119293930-119294380 | Common:1; Rare:98 | ||||
| chr3:119463538-119464026 | Common:27; Rare:502 | ||||
| chr3:119468429-119468679 | Common:4; Rare:84 | ||||
| chr3:119468720-119469060 | Common:4; Rare:559; Clinvar (pathogenic):3 | ||||
| chr3:119469210-119469790 | Common:4; Rare:187 | ||||
| chr3:119498336-119498734 | Common:40; Rare:886 |