| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44891331-44891950 | Common:6; Rare:224 | ||||
| chr19:44905382-44905782 | Common:2; Rare:96; Clinvar:2 | ||||
| chr19:44905684-44905865 | Common:1; Rare:93 | ||||
| chr19:44906210-44906842 | Common:5; Rare:469 | ||||
| chr19:44913609-44914084 | Common:3; Rare:106 | ||||
| chr19:44914004-44914440 | Common:12; Rare:268 | ||||
| chr19:44914351-44915441 | Common:38; Rare:1240 | ||||
| chr19:44948214-44948614 | Common:9; Rare:161; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:44954597-44955167 | Common:15; Rare:547 | ||||
| chr19:44955126-44955526 | Common:22; Rare:524 | ||||
| chr19:45001210-45001610 | Common:2; Rare:257 | ||||
| chr19:45001573-45002250 | Common:14; Rare:325 | ||||
| chr19:45038808-45039208 | Rare:462 | ||||
| chr19:45039281-45040195 | Common:10; Rare:351 | ||||
| chr19:45075626-45076478 | Common:6; Rare:373 |