| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2800870-2801301 | Common:2; Rare:109 | ||||
| chr12:2812607-2812752 | Common:1; Rare:55 | ||||
| chr12:2812886-2812945 | Rare:22 | ||||
| chr12:2877027-2877271 | Rare:76 | ||||
| chr12:3077267-3077428 | Common:5; Rare:71 | ||||
| chr12:3753049-3753219 | Common:1; Rare:45 | ||||
| chr12:4320982-4321258 | Common:5; Rare:104 | ||||
| chr12:4538431-4538930 | Common:3; Rare:114 | ||||
| chr12:4649045-4649173 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr12:4720060-4720496 | Common:2; Rare:90 | ||||
| chr12:6200059-6200479 | Common:4; Rare:121 | ||||
| chr12:6232429-6232718 | Common:1; Rare:60 | ||||
| chr12:6310234-6310265 | Rare:4 | ||||
| chr12:6310546-6310768 | Common:4; Rare:54 | ||||
| chr12:6317573-6317893 | Common:3; Rare:96 |