| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335601-46335792 | Common:4; Rare:89; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46762476-46762669 | Common:3; Rare:73 | ||||
| chr22:50085290-50085494 | Common:3; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50185666-50185942 | Common:5; Rare:110 | ||||
| chr22:50244950-50245080 | Common:2; Rare:49 | ||||
| chr22:50326929-50327185 | Common:3; Rare:85 | ||||
| chr22:50525531-50525710 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50628092-50628280 | Common:9; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783878 | Common:2; Rare:94 | ||||
| chr3:196707-197054 | Common:2; Rare:112 | ||||
| chr3:197059-197341 | Common:3; Rare:97 | ||||
| chr3:197388-197824 | Common:7; Rare:155 | ||||
| chr3:197866-198034 | Common:2; Rare:51 | ||||
| chr3:1092777-1093120 | Common:1; Rare:93 | ||||
| chr3:2098583-2098967 | Common:4; Rare:153 |