| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119660872-119661098 | Rare:37 | ||||
| chr3:119677297-119677519 | Common:1; Rare:83 | ||||
| chr3:120093488-120093893 | Rare:105 | ||||
| chr3:120094341-120094375 | Rare:12 | ||||
| chr3:120094376-120094752 | Common:4; Rare:124 | ||||
| chr3:120349296-120349449 | Common:2; Rare:52 | ||||
| chr3:120450817-120450874 | Common:1; Rare:20 | ||||
| chr3:120450885-120451123 | Rare:80 | ||||
| chr3:120742503-120742771 | Common:2; Rare:75 | ||||
| chr3:121749209-121749308 | Rare:23 | ||||
| chr3:121749467-121749515 | Rare:7 | ||||
| chr3:121749646-121750074 | Common:2; Rare:107 | ||||
| chr3:121834960-121835244 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383190-122383323 | Common:1; Rare:42 | ||||
| chr3:122384036-122384258 | Rare:80 |