| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10796063-10796340 | Rare:69; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:10798386-10798572 | Rare:60; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:10829956-10830181 | Common:1; Rare:61; Clinvar (benign):2 | ||||
| chr19:10836297-10836532 | Common:2; Rare:56 | ||||
| chr19:10928537-10928815 | Common:2; Rare:83 | ||||
| chr19:10960689-10961141 | Common:3; Rare:168; Clinvar (benign):1 | ||||
| chr19:11197485-11197633 | Common:1; Rare:38 | ||||
| chr19:11374889-11375252 | Common:1; Rare:114 | ||||
| chr19:11435517-11435761 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11559195-11559407 | Common:1; Rare:66 | ||||
| chr19:11578888-11579302 | Common:3; Rare:78 | ||||
| chr19:11738857-11739242 | Common:4; Rare:103 | ||||
| chr19:12035660-12035861 | Common:1; Rare:73 | ||||
| chr19:12551376-12551732 | Common:2; Rare:97 | ||||
| chr19:12610682-12611063 | Common:1; Rare:117 |