| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35510244-35510665 | Common:1; Rare:91 | ||||
| chr19:35545417-35545720 | Common:4; Rare:95 | ||||
| chr19:35545877-35546129 | Rare:83 | ||||
| chr19:35612592-35612858 | Common:2; Rare:84 | ||||
| chr19:35628506-35629154 | Common:6; Rare:170 | ||||
| chr19:35643291-35643448 | Common:1; Rare:58 | ||||
| chr19:35643455-35643558 | Rare:40 | ||||
| chr19:35643691-35643944 | Common:2; Rare:70 | ||||
| chr19:35648056-35648414 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35717364-35717811 | Common:4; Rare:100 | ||||
| chr19:35717829-35718082 | Rare:76 | ||||
| chr19:35740454-35740919 | Common:6; Rare:165 | ||||
| chr19:35740935-35741180 | Rare:97 | ||||
| chr19:35741333-35741372 | Rare:11 | ||||
| chr19:35744884-35745191 | Common:3; Rare:102 |