| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501565-21501857 | Common:1; Rare:71 | ||||
| chr12:21941195-21941325 | Rare:26 | ||||
| chr12:22544488-22544721 | Common:1; Rare:50 | ||||
| chr12:22625023-22625235 | Rare:110 | ||||
| chr12:25195084-25195299 | Common:2; Rare:68 | ||||
| chr12:26938014-26938534 | Common:8; Rare:174 | ||||
| chr12:27523989-27524245 | Rare:62 | ||||
| chr12:27710727-27710875 | Common:2; Rare:61 | ||||
| chr12:28190378-28190489 | Common:1; Rare:32 | ||||
| chr12:31073738-31073892 | Common:7; Rare:58 | ||||
| chr12:31729012-31729267 | Rare:74 | ||||
| chr12:31959282-31959488 | Common:2; Rare:65 | ||||
| chr12:38905580-38905672 | Common:3; Rare:27 | ||||
| chr12:40224957-40225084 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr12:40225282-40225423 | Rare:40 |