| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57488806-57489043 | Common:3; Rare:47; Clinvar (benign):1 | ||||
| chr12:57720497-57720964 | Common:1; Rare:119 | ||||
| chr12:57772092-57772251 | Rare:54 | ||||
| chr12:62260119-62260407 | Common:1; Rare:107 | ||||
| chr12:64759097-64759472 | Rare:119; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:66130712-66130792 | Rare:29 | ||||
| chr12:76348382-76348481 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559764-76559896 | Rare:54 | ||||
| chr12:77065523-77065713 | Rare:66 | ||||
| chr12:79935134-79935363 | Rare:82 | ||||
| chr12:82358363-82358552 | Rare:79 | ||||
| chr12:88142050-88142315 | Rare:63; Clinvar:3 | ||||
| chr12:88580467-88580543 | Common:1; Rare:25 | ||||
| chr12:89524748-89524896 | Common:1; Rare:27 | ||||
| chr12:89708673-89708998 | Rare:116 |