| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1073280-1073680 | Common:1; Rare:176 | ||||
| chr19:1082520-1082884 | Common:8; Rare:213 | ||||
| chr19:1095229-1095629 | Common:32; Rare:545 | ||||
| chr19:1095763-1096163 | Common:4; Rare:77 | ||||
| chr19:1103644-1104125 | Common:51; Rare:1101 | ||||
| chr19:1104394-1104821 | Common:11; Rare:245 | ||||
| chr19:1105230-1105703 | Common:5; Rare:326; Clinvar (pathogenic):2 | ||||
| chr19:1132070-1132480 | Common:3; Rare:460 | ||||
| chr19:1172924-1174016 | Common:7; Rare:468 | ||||
| chr19:1174122-1174522 | Common:10; Rare:694 | ||||
| chr19:1205351-1205951 | Common:11; Rare:677; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:1207151-1207977 | Common:4; Rare:530; Clinvar:2; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr19:1237682-1238351 | Common:10; Rare:696 | ||||
| chr19:1241480-1241940 | Rare:560 | ||||
| chr19:1244356-1245150 | Common:7; Rare:305 |