| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:401438-401666 | Rare:62 | ||||
| chr12:643624-643757 | Rare:25 | ||||
| chr12:991120-991307 | Common:3; Rare:88 | ||||
| chr12:2004420-2004669 | Common:2; Rare:80 | ||||
| chr12:2876923-2877268 | Common:1; Rare:106 | ||||
| chr12:2890717-2890938 | Common:1; Rare:84 | ||||
| chr12:3077267-3077428 | Common:5; Rare:71 | ||||
| chr12:3873355-3873535 | Common:1; Rare:40 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538448-4538942 | Common:3; Rare:113 | ||||
| chr12:4649016-4649149 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr12:6200031-6200475 | Common:4; Rare:126 | ||||
| chr12:6383953-6384256 | Common:1; Rare:68 | ||||
| chr12:6493234-6493502 | Common:7; Rare:79 | ||||
| chr12:6493763-6494154 | Common:2; Rare:116 |