| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:20369558-20369991 | Common:4; Rare:188 | ||||
| chr12:20370015-20370244 | Rare:82 | ||||
| chr12:21437578-21437733 | Common:5; Rare:63 | ||||
| chr12:21501505-21501880 | Common:4; Rare:103 | ||||
| chr12:21526248-21526478 | Rare:45 | ||||
| chr12:21657750-21657998 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774786-21775001 | Rare:45 | ||||
| chr12:21941195-21941445 | Rare:61 | ||||
| chr12:22544154-22544292 | Common:1; Rare:68 | ||||
| chr12:22624870-22625257 | Common:2; Rare:154 | ||||
| chr12:24948999-24949187 | Common:1; Rare:50 | ||||
| chr12:25195155-25195338 | Common:1; Rare:54 | ||||
| chr12:25959350-25959387 | Common:1; Rare:12 | ||||
| chr12:26937936-26938577 | Common:11; Rare:212 | ||||
| chr12:27022412-27022610 | Common:2; Rare:62 |