| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114056182-114056345 | Common:1; Rare:41 | ||||
| chr3:114056467-114056985 | Common:2; Rare:183 | ||||
| chr3:114291349-114291727 | Common:3; Rare:67 | ||||
| chr3:114454386-114454440 | Rare:15 | ||||
| chr3:114454832-114454915 | Rare:7 | ||||
| chr3:115100258-115100483 | Common:1; Rare:46 | ||||
| chr3:115146620-115146798 | Rare:54 | ||||
| chr3:119240132-119240501 | Common:4; Rare:83 | ||||
| chr3:119240598-119240817 | Common:1; Rare:63 | ||||
| chr3:119240845-119241104 | Common:1; Rare:69 | ||||
| chr3:119294061-119294298 | Rare:53 | ||||
| chr3:119294468-119294743 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:119463538-119464010 | Common:6; Rare:115 | ||||
| chr3:119468793-119469047 | Common:1; Rare:93; Clinvar (pathogenic):1 | ||||
| chr3:119498349-119498734 | Common:5; Rare:126 |