| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335601-46335752 | Common:2; Rare:63; Clinvar:6; Clinvar (benign):6 | ||||
| chr22:46762506-46762669 | Common:3; Rare:58 | ||||
| chr22:50783601-50783859 | Common:2; Rare:79 | ||||
| chr3:4303160-4303405 | Common:2; Rare:76 | ||||
| chr3:4493176-4493350 | Rare:62 | ||||
| chr3:4979201-4979530 | Common:2; Rare:73 | ||||
| chr3:8501649-8501947 | Common:2; Rare:108 | ||||
| chr3:9249624-9249816 | Common:2; Rare:46 | ||||
| chr3:9363004-9363098 | Rare:33 | ||||
| chr3:9397437-9397688 | Common:1; Rare:92 | ||||
| chr3:9792414-9792552 | Rare:37 | ||||
| chr3:9792692-9792729 | Rare:12 | ||||
| chr3:9792789-9793118 | Common:3; Rare:114 | ||||
| chr3:9843986-9844126 | Common:2; Rare:51 | ||||
| chr3:9917012-9917147 | Common:1; Rare:27 |