| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:85836315-85836386 | Rare:7 | ||||
| chr12:88035426-88035630 | Common:1; Rare:67 | ||||
| chr12:88035761-88035812 | Rare:18 | ||||
| chr12:88141970-88142412 | Rare:122; Clinvar:5 | ||||
| chr12:88142801-88142900 | Rare:17 | ||||
| chr12:88580276-88580622 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr12:88580677-88580865 | Rare:45 | ||||
| chr12:89351533-89351879 | Common:2; Rare:120 | ||||
| chr12:89352233-89352830 | Common:5; Rare:165 | ||||
| chr12:89353014-89353116 | Rare:20 | ||||
| chr12:89353293-89353542 | Rare:65 | ||||
| chr12:89353618-89353838 | Common:4; Rare:60 | ||||
| chr12:89524533-89524594 | Rare:26 | ||||
| chr12:89524697-89524928 | Common:2; Rare:51 | ||||
| chr12:89525422-89525661 | Common:1; Rare:59 |