| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064449-104064555 | Rare:27 | ||||
| chr12:105107609-105107789 | Common:1; Rare:81 | ||||
| chr12:105236072-105236304 | Common:2; Rare:107 | ||||
| chr12:106987049-106987258 | Common:4; Rare:60 | ||||
| chr12:108562439-108562699 | Common:9; Rare:112; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109477275-109477664 | Common:3; Rare:101 | ||||
| chr12:109573451-109573813 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880658 | Common:1; Rare:90 | ||||
| chr12:110468665-110468909 | Rare:62 | ||||
| chr12:110502058-110502195 | Common:1; Rare:51 | ||||
| chr12:110614057-110614203 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685761-111686085 | Rare:122 | ||||
| chr12:112013134-112013468 | Common:1; Rare:116 | ||||
| chr12:113185447-113185748 | Common:7; Rare:109 | ||||
| chr12:114406035-114406233 | Common:1; Rare:47 |