| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783606-50783876 | Common:2; Rare:81 | ||||
| chr3:3126775-3126984 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr3:4303279-4303405 | Common:1; Rare:54 | ||||
| chr3:8501641-8501911 | Common:1; Rare:99 | ||||
| chr3:9363020-9363098 | Rare:27 | ||||
| chr3:9397437-9397924 | Common:1; Rare:152 | ||||
| chr3:9731449-9731831 | Common:3; Rare:124 | ||||
| chr3:9792363-9792610 | Rare:68 | ||||
| chr3:9792732-9793124 | Common:3; Rare:135 | ||||
| chr3:9843963-9844137 | Common:2; Rare:72 | ||||
| chr3:9916896-9917154 | Common:3; Rare:60 | ||||
| chr3:9933507-9933899 | Common:3; Rare:155; Clinvar:3 | ||||
| chr3:10026335-10026480 | Rare:42 | ||||
| chr3:10115520-10115748 | Common:3; Rare:82 | ||||
| chr3:11154362-11154542 | Common:3; Rare:45 |