| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31073761-31073907 | Common:7; Rare:55 | ||||
| chr12:31326111-31326462 | Common:4; Rare:121 | ||||
| chr12:31729012-31729267 | Rare:74 | ||||
| chr12:31959293-31959488 | Common:2; Rare:64 | ||||
| chr12:32679086-32679350 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:32755248-32755366 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:34022360-34022514 | Common:2; Rare:48 | ||||
| chr12:42238200-42238483 | Rare:100 | ||||
| chr12:42326065-42326205 | Common:1; Rare:42 | ||||
| chr12:43758749-43759020 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806249-43806412 | Common:2; Rare:55 | ||||
| chr12:45215993-45216163 | Rare:57 | ||||
| chr12:45990543-45990933 | Common:2; Rare:125 | ||||
| chr12:46372714-46373016 | Common:1; Rare:121 | ||||
| chr12:47705970-47706088 | Rare:55 |