| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004420-2004669 | Common:2; Rare:80 | ||||
| chr12:2812610-2812713 | Common:1; Rare:32 | ||||
| chr12:2877042-2877260 | Rare:65 | ||||
| chr12:4648971-4649149 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr12:6383995-6384262 | Common:1; Rare:59 | ||||
| chr12:6493230-6493377 | Common:6; Rare:41 | ||||
| chr12:6493774-6494126 | Common:2; Rare:105 | ||||
| chr12:6534245-6534582 | Common:6; Rare:133 | ||||
| chr12:6568249-6568371 | Rare:45 | ||||
| chr12:6724086-6724172 | Rare:26 | ||||
| chr12:6851902-6852174 | Rare:70 | ||||
| chr12:6867379-6867665 | Common:2; Rare:137; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873334-6873541 | Common:1; Rare:55 | ||||
| chr12:6970610-6970952 | Common:3; Rare:105 | ||||
| chr12:7108375-7108681 | Common:2; Rare:96 |