| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50582818-50583120 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628091-50628263 | Common:8; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783611-50783859 | Common:2; Rare:74 | ||||
| chr3:197010-197332 | Common:3; Rare:111 | ||||
| chr3:2098637-2098969 | Common:4; Rare:131 | ||||
| chr3:4303253-4303423 | Common:1; Rare:66 | ||||
| chr3:4493176-4493532 | Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:8501638-8501941 | Common:2; Rare:111 | ||||
| chr3:9249624-9249748 | Common:1; Rare:35 | ||||
| chr3:9362978-9363127 | Common:1; Rare:55 | ||||
| chr3:9397432-9397692 | Common:1; Rare:98 | ||||
| chr3:9749814-9750009 | Common:1; Rare:65 | ||||
| chr3:9769888-9770037 | Common:1; Rare:40 | ||||
| chr3:9792376-9792570 | Rare:55 | ||||
| chr3:9792701-9793115 | Common:3; Rare:145 |