| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335619-46335767 | Common:2; Rare:62; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762438-46762669 | Common:3; Rare:91 | ||||
| chr22:50244972-50245048 | Common:1; Rare:30 | ||||
| chr22:50582818-50583120 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628122-50628228 | Common:7; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50783606-50783864 | Common:2; Rare:76 | ||||
| chr3:3126775-3126984 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr3:4303253-4303405 | Common:1; Rare:58 | ||||
| chr3:4493165-4493348 | Rare:65 | ||||
| chr3:4980296-4980517 | Rare:49 | ||||
| chr3:8501653-8501854 | Rare:69 | ||||
| chr3:9249549-9249743 | Common:1; Rare:43 | ||||
| chr3:9362978-9363117 | Common:1; Rare:53 | ||||
| chr3:9792398-9792529 | Rare:38 | ||||
| chr3:9792705-9793124 | Common:3; Rare:148 |