| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2876984-2877262 | Rare:84 | ||||
| chr12:2890692-2890935 | Common:1; Rare:96 | ||||
| chr12:2959240-2959433 | Rare:52 | ||||
| chr12:2959824-2959944 | Common:1; Rare:32 | ||||
| chr12:3077233-3077438 | Common:7; Rare:90 | ||||
| chr12:3873355-3873525 | Common:1; Rare:39 | ||||
| chr12:4273460-4273843 | Rare:101 | ||||
| chr12:4320934-4321266 | Common:5; Rare:129 | ||||
| chr12:4538431-4538934 | Common:3; Rare:115 | ||||
| chr12:4649045-4649178 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr12:6200042-6200521 | Common:4; Rare:139 | ||||
| chr12:6384002-6384234 | Common:1; Rare:50 | ||||
| chr12:6493141-6493503 | Common:8; Rare:112 | ||||
| chr12:6493746-6494140 | Common:2; Rare:116 | ||||
| chr12:6534232-6534602 | Common:6; Rare:142 |