| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004427-2004666 | Common:2; Rare:74 | ||||
| chr12:2796950-2797280 | Rare:80 | ||||
| chr12:2800857-2801311 | Common:2; Rare:116 | ||||
| chr12:2812553-2812754 | Common:1; Rare:65 | ||||
| chr12:2812880-2813036 | Rare:46 | ||||
| chr12:2877027-2877268 | Rare:75 | ||||
| chr12:3077267-3077447 | Common:6; Rare:78 | ||||
| chr12:3873307-3873533 | Common:4; Rare:47 | ||||
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4538436-4538930 | Common:3; Rare:112 | ||||
| chr12:4649010-4649178 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:6200005-6200559 | Common:4; Rare:166 | ||||
| chr12:6310584-6310776 | Common:4; Rare:46 | ||||
| chr12:6341922-6342123 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6374755-6375172 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):3 |