| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46053789-46053859 | Rare:25 | ||||
| chr22:46250262-46250432 | Common:3; Rare:56 | ||||
| chr22:46762526-46762676 | Common:3; Rare:51 | ||||
| chr22:49918265-49918731 | Common:4; Rare:165; Clinvar (benign):3 | ||||
| chr22:50582397-50582455 | Rare:31 | ||||
| chr22:50582780-50583185 | Common:9; Rare:145; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628046-50628278 | Common:9; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783598-50783822 | Common:2; Rare:73 | ||||
| chr3:8501644-8501944 | Common:2; Rare:108 | ||||
| chr3:9362977-9363124 | Common:1; Rare:55 | ||||
| chr3:9397437-9397597 | Rare:57 | ||||
| chr3:9749812-9750064 | Common:1; Rare:81 | ||||
| chr3:9792364-9792570 | Rare:59 | ||||
| chr3:9792682-9793119 | Common:3; Rare:153 | ||||
| chr3:9986774-9987169 | Common:4; Rare:111 |