| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120117559-120117610 | Rare:10 | ||||
| chr12:120194477-120194860 | Common:1; Rare:130 | ||||
| chr12:120194912-120195249 | Common:3; Rare:68 | ||||
| chr12:120201059-120201531 | Common:2; Rare:137 | ||||
| chr12:120201552-120201683 | Rare:25 | ||||
| chr12:120265667-120266034 | Common:1; Rare:117 | ||||
| chr12:120302020-120302392 | Common:2; Rare:68 | ||||
| chr12:120302549-120302584 | Common:1; Rare:8 | ||||
| chr12:120368293-120368566 | Common:2; Rare:66 | ||||
| chr12:120368972-120369090 | Rare:25 | ||||
| chr12:120369153-120369370 | Common:1; Rare:54 | ||||
| chr12:120437783-120438169 | Common:2; Rare:127; Clinvar (benign):2 | ||||
| chr12:120446113-120446166 | Rare:8 | ||||
| chr12:120446286-120446584 | Common:3; Rare:118 | ||||
| chr12:120446629-120446791 | Common:2; Rare:57 |