| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:401446-401657 | Rare:56 | ||||
| chr12:610367-610480 | Rare:11 | ||||
| chr12:643609-643748 | Rare:26 | ||||
| chr12:991080-991322 | Common:4; Rare:110 | ||||
| chr12:2004420-2004495 | Rare:31 | ||||
| chr12:2812475-2812733 | Common:1; Rare:67 | ||||
| chr12:2877039-2877253 | Rare:64 | ||||
| chr12:2959798-2959944 | Common:1; Rare:39 | ||||
| chr12:3873355-3873527 | Common:1; Rare:39 | ||||
| chr12:4273456-4273843 | Rare:102 | ||||
| chr12:4275452-4275578 | Common:2; Rare:18 | ||||
| chr12:4320991-4321258 | Common:4; Rare:100 | ||||
| chr12:4538444-4538907 | Common:1; Rare:102 | ||||
| chr12:4649030-4649171 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr12:6493208-6493386 | Common:6; Rare:49 |