| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:112990787-112991012 | Common:2; Rare:73 | ||||
| chr3:113019350-113019518 | Common:4; Rare:40 | ||||
| chr3:113019634-113019825 | Common:2; Rare:66 | ||||
| chr3:113211453-113211769 | Common:6; Rare:73 | ||||
| chr3:113515086-113515261 | Common:1; Rare:53 | ||||
| chr3:113746150-113746332 | Rare:73 | ||||
| chr3:113746770-113747120 | Common:4; Rare:75 | ||||
| chr3:114056486-114056823 | Common:2; Rare:130 | ||||
| chr3:114454666-114454870 | Rare:23 | ||||
| chr3:115100261-115100408 | Rare:25 | ||||
| chr3:119240856-119241180 | Common:1; Rare:78 | ||||
| chr3:119293738-119294143 | Common:1; Rare:82 | ||||
| chr3:119294695-119294752 | Common:1; Rare:12; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:119463598-119463817 | Common:3; Rare:66 | ||||
| chr3:119468826-119469015 | Rare:69 |