| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41621027-41621368 | Common:7; Rare:129 | ||||
| chr22:41947093-41947179 | Rare:33 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42649303-42649479 | Common:1; Rare:66 | ||||
| chr22:45163792-45163940 | Common:2; Rare:50 | ||||
| chr22:46250268-46250396 | Common:1; Rare:39 | ||||
| chr22:49918283-49918739 | Common:5; Rare:161; Clinvar (benign):3 | ||||
| chr22:50582785-50583124 | Common:7; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628046-50628276 | Common:9; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783618-50783821 | Common:2; Rare:62 | ||||
| chr3:8501653-8501859 | Rare:70 | ||||
| chr3:9363018-9363098 | Rare:29 | ||||
| chr3:9792409-9792511 | Rare:29 | ||||
| chr3:9793006-9793119 | Common:2; Rare:52 | ||||
| chr3:9933510-9933863 | Common:2; Rare:142; Clinvar:3 |