| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120908086-120908244 | Rare:48 | ||||
| chr3:121749445-121749509 | Rare:12 | ||||
| chr3:121749643-121750021 | Common:1; Rare:87 | ||||
| chr3:121834972-121835269 | Common:3; Rare:100; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383180-122383308 | Common:1; Rare:42 | ||||
| chr3:122384054-122384268 | Rare:79 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122514853-122515034 | Common:1; Rare:51 | ||||
| chr3:122564236-122564436 | Common:3; Rare:59 | ||||
| chr3:122680660-122680952 | Rare:91 | ||||
| chr3:123585035-123585117 | Common:1; Rare:38 | ||||
| chr3:123585489-123585590 | Rare:20 | ||||
| chr3:123620418-123620880 | Common:3; Rare:70 | ||||
| chr3:123649160-123649254 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):10 | ||||
| chr3:123700912-123701321 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):2 |