| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6873274-6873739 | Common:8; Rare:244 | ||||
| chr12:6904570-6904870 | Common:2; Rare:122 | ||||
| chr12:6914207-6914627 | Rare:140 | ||||
| chr12:6927628-6928011 | Common:2; Rare:132 | ||||
| chr12:6943486-6943818 | Common:8; Rare:262 | ||||
| chr12:6943824-6944148 | Common:19; Rare:519; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:6946286-6946649 | Common:1; Rare:95 | ||||
| chr12:6970512-6971080 | Common:13; Rare:334; Clinvar (benign):3 | ||||
| chr12:7018372-7018645 | Common:2; Rare:131 | ||||
| chr12:7108468-7108701 | Common:1; Rare:64 | ||||
| chr12:7109120-7109301 | Rare:57 | ||||
| chr12:7127780-7128280 | Rare:144 | ||||
| chr12:7128833-7129210 | Common:3; Rare:70 | ||||
| chr12:7129993-7130459 | Common:11; Rare:171 | ||||
| chr12:7189551-7189743 | Rare:70; Clinvar:4 |