| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723970-6724177 | Rare:55 | ||||
| chr12:6752937-6753189 | Common:6; Rare:77 | ||||
| chr12:6851917-6852174 | Rare:65 | ||||
| chr12:6867391-6867569 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873291-6873532 | Common:1; Rare:72 | ||||
| chr12:6904723-6904847 | Rare:35 | ||||
| chr12:6970602-6970977 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr12:7018459-7018571 | Common:1; Rare:33 | ||||
| chr12:7108448-7108600 | Common:1; Rare:50 | ||||
| chr12:7109161-7109575 | Common:2; Rare:101 | ||||
| chr12:7128885-7129034 | Common:1; Rare:19 | ||||
| chr12:7130240-7130418 | Common:5; Rare:47 | ||||
| chr12:7155583-7155887 | Common:1; Rare:46 | ||||
| chr12:7189551-7189735 | Rare:67; Clinvar:4 | ||||
| chr12:8032589-8032793 | Rare:71 |