| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2812524-2812742 | Common:1; Rare:64 | ||||
| chr12:2812880-2812958 | Rare:29 | ||||
| chr12:2877039-2877253 | Rare:64 | ||||
| chr12:2959846-2959944 | Common:1; Rare:25 | ||||
| chr12:3077240-3077447 | Common:7; Rare:89 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4275455-4275569 | Common:2; Rare:15 | ||||
| chr12:4275749-4276061 | Rare:65 | ||||
| chr12:4320943-4321260 | Common:5; Rare:121 | ||||
| chr12:4538440-4538907 | Common:1; Rare:102 | ||||
| chr12:4649010-4649154 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr12:6124445-6124762 | Rare:46; Clinvar:2 | ||||
| chr12:6124893-6124978 | Rare:24 | ||||
| chr12:6200005-6200480 | Common:4; Rare:138 | ||||
| chr12:6310495-6310749 | Common:4; Rare:67 |