| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46053778-46053901 | Rare:43 | ||||
| chr22:46250268-46250408 | Common:1; Rare:45 | ||||
| chr22:46267841-46268042 | Common:1; Rare:65 | ||||
| chr22:46335601-46335797 | Common:5; Rare:91; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762506-46762705 | Common:3; Rare:73 | ||||
| chr22:50185683-50185942 | Common:4; Rare:107 | ||||
| chr22:50244954-50245108 | Common:2; Rare:61 | ||||
| chr22:50525547-50525718 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50532484-50532663 | Common:2; Rare:41 | ||||
| chr22:50582412-50582441 | Rare:12 | ||||
| chr22:50582818-50583136 | Common:5; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628082-50628270 | Common:8; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783601-50783883 | Common:2; Rare:88 | ||||
| chr3:196707-196883 | Rare:57 | ||||
| chr3:197119-197319 | Common:1; Rare:65 |