| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:26937956-26938541 | Common:11; Rare:194 | ||||
| chr12:27243973-27244304 | Common:2; Rare:105 | ||||
| chr12:27523980-27524227 | Rare:64 | ||||
| chr12:27710738-27710846 | Common:1; Rare:44 | ||||
| chr12:28190378-28190481 | Common:1; Rare:29 | ||||
| chr12:29381141-29381379 | Common:3; Rare:74 | ||||
| chr12:30754852-30755049 | Rare:82 | ||||
| chr12:31073760-31073892 | Common:6; Rare:52 | ||||
| chr12:31074085-31074240 | Rare:30 | ||||
| chr12:31324143-31324316 | Rare:36 | ||||
| chr12:31326058-31326456 | Common:4; Rare:132 | ||||
| chr12:31729019-31729292 | Common:1; Rare:82 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32501980-32502249 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679050-32679335 | Common:2; Rare:107; Clinvar (benign):2 |