| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121545973-121546089 | Common:1; Rare:29 | ||||
| chr3:121834956-121835244 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383332 | Common:1; Rare:43 | ||||
| chr3:122384041-122384247 | Rare:76 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122514873-122515006 | Common:1; Rare:38 | ||||
| chr3:122564006-122564227 | Common:1; Rare:47 | ||||
| chr3:122564236-122564468 | Common:3; Rare:69 | ||||
| chr3:123201829-123201962 | Common:1; Rare:44 | ||||
| chr3:123585036-123585284 | Common:1; Rare:77 | ||||
| chr3:123585489-123585585 | Rare:18 | ||||
| chr3:123620357-123620411 | Rare:16 | ||||
| chr3:123620418-123620881 | Common:3; Rare:70 | ||||
| chr3:123700936-123701321 | Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:125375209-125375389 | Rare:46 |