| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76559715-76559902 | Rare:74 | ||||
| chr12:77065551-77065653 | Rare:30 | ||||
| chr12:79935080-79935362 | Rare:105 | ||||
| chr12:82358372-82358554 | Rare:76 | ||||
| chr12:82358747-82358899 | Common:3; Rare:77 | ||||
| chr12:88580439-88580550 | Common:1; Rare:40 | ||||
| chr12:89524742-89524874 | Common:1; Rare:23 | ||||
| chr12:89708818-89708971 | Rare:62 | ||||
| chr12:91182612-91182916 | Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:92145818-92146113 | Common:3; Rare:99 | ||||
| chr12:93570827-93571057 | Rare:60 | ||||
| chr12:95858841-95858946 | Rare:15 | ||||
| chr12:98593469-98593765 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:101407731-101408035 | Common:2; Rare:73 | ||||
| chr12:102120051-102120249 | Rare:76 |