| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:108589584-108589710 | Common:1; Rare:28 | ||||
| chr3:112561628-112561689 | Rare:22 | ||||
| chr3:112561905-112562072 | Rare:54 | ||||
| chr3:112990853-112990994 | Common:1; Rare:50 | ||||
| chr3:113746147-113746328 | Rare:71 | ||||
| chr3:113746966-113747083 | Common:3; Rare:16 | ||||
| chr3:114056481-114056825 | Common:2; Rare:131 | ||||
| chr3:115100258-115100380 | Rare:20 | ||||
| chr3:120094436-120094762 | Common:3; Rare:101 | ||||
| chr3:120742511-120742777 | Common:2; Rare:74 | ||||
| chr3:121834989-121835234 | Common:3; Rare:80; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383207-122383308 | Common:1; Rare:30 | ||||
| chr3:122384076-122384247 | Rare:66 | ||||
| chr3:122514873-122515016 | Common:1; Rare:40 | ||||
| chr3:123201837-123201962 | Common:1; Rare:42 |