| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105188399-105188714 | Common:1; Rare:61 | ||||
| chr12:105195477-105195717 | Common:1; Rare:77 | ||||
| chr12:105235981-105236300 | Common:3; Rare:126 | ||||
| chr12:106247432-106247599 | Common:2; Rare:55 | ||||
| chr12:106357730-106357837 | Common:2; Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:106955477-106955913 | Common:3; Rare:162 | ||||
| chr12:106956657-106956799 | Rare:24 | ||||
| chr12:106970839-106971150 | Common:1; Rare:58 | ||||
| chr12:106985219-106985305 | Rare:15 | ||||
| chr12:106987036-106987232 | Common:4; Rare:58 | ||||
| chr12:107093490-107093661 | Rare:62 | ||||
| chr12:107685706-107685956 | Rare:83 | ||||
| chr12:108515044-108515319 | Common:1; Rare:82 | ||||
| chr12:108537577-108537644 | Rare:18 | ||||
| chr12:108561117-108561486 | Common:4; Rare:97 |