| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120093472-120093920 | Rare:128 | ||||
| chr3:120094429-120094771 | Common:4; Rare:108 | ||||
| chr3:120742503-120742771 | Common:2; Rare:75 | ||||
| chr3:121545986-121546158 | Common:1; Rare:38 | ||||
| chr3:121749630-121750028 | Common:1; Rare:91 | ||||
| chr3:121834983-121835234 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383190-122383332 | Common:1; Rare:44 | ||||
| chr3:122384063-122384268 | Rare:75 | ||||
| chr3:122416075-122416218 | Rare:40 | ||||
| chr3:122514828-122515013 | Common:2; Rare:56 | ||||
| chr3:122564236-122564429 | Common:3; Rare:57 | ||||
| chr3:122793755-122793908 | Common:3; Rare:43 | ||||
| chr3:123585489-123585582 | Rare:16 | ||||
| chr3:123620448-123620879 | Common:3; Rare:65 | ||||
| chr3:123700936-123701321 | Rare:82; Clinvar:4; Clinvar (benign):1 |