| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45413565-45413745 | Common:1; Rare:76 | ||||
| chr22:46053749-46053901 | Rare:57 | ||||
| chr22:46250254-46250404 | Common:2; Rare:45 | ||||
| chr22:46267841-46268032 | Common:1; Rare:58 | ||||
| chr22:46296672-46296924 | Common:2; Rare:90 | ||||
| chr22:46335616-46335792 | Common:4; Rare:82; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46762503-46762669 | Common:3; Rare:60 | ||||
| chr22:50244960-50245054 | Common:2; Rare:38 | ||||
| chr22:50507944-50508297 | Common:4; Rare:98 | ||||
| chr22:50582790-50583120 | Common:7; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628034-50628301 | Common:9; Rare:119; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783598-50783859 | Common:2; Rare:82 | ||||
| chr3:3126816-3127026 | Common:4; Rare:95; Clinvar (benign):4 | ||||
| chr3:3179666-3179840 | Common:2; Rare:65; Clinvar:3 | ||||
| chr3:4467235-4467323 | Rare:36; Clinvar:1; Clinvar (benign):1 |