| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121545941-121546089 | Common:1; Rare:42 | ||||
| chr3:121749643-121750068 | Common:2; Rare:105 | ||||
| chr3:121834956-121835238 | Common:3; Rare:90; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122382947-122383354 | Common:2; Rare:118 | ||||
| chr3:122384030-122384275 | Common:2; Rare:85 | ||||
| chr3:122416039-122416257 | Common:1; Rare:71 | ||||
| chr3:122514840-122515029 | Common:2; Rare:54 | ||||
| chr3:122564169-122564429 | Common:4; Rare:71 | ||||
| chr3:122564437-122564591 | Common:1; Rare:42 | ||||
| chr3:122680664-122680874 | Rare:62 | ||||
| chr3:122681067-122681278 | Rare:56 | ||||
| chr3:122793685-122793745 | Common:1; Rare:20 | ||||
| chr3:122793777-122794084 | Common:3; Rare:65 | ||||
| chr3:123066931-123067156 | Rare:58 | ||||
| chr3:123201837-123201984 | Common:1; Rare:51 |