| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50628082-50628289 | Common:9; Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783606-50783822 | Common:2; Rare:66 | ||||
| chr3:8501558-8501888 | Common:2; Rare:121 | ||||
| chr3:9249631-9249757 | Common:1; Rare:35 | ||||
| chr3:9362945-9363093 | Common:2; Rare:55 | ||||
| chr3:9397437-9397694 | Common:1; Rare:94 | ||||
| chr3:9749779-9749991 | Rare:70 | ||||
| chr3:9792373-9792600 | Rare:64 | ||||
| chr3:9792732-9793121 | Common:3; Rare:134 | ||||
| chr3:9933514-9933863 | Common:2; Rare:142; Clinvar:3 | ||||
| chr3:10026294-10026414 | Rare:43 | ||||
| chr3:12664101-12664323 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124733-14125156 | Common:4; Rare:121; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178529-14178858 | Common:2; Rare:171; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402433-14402576 | Rare:36 |