| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79988274-79988638 | Common:3; Rare:119; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr18:80034084-80034521 | Common:6; Rare:154 | ||||
| chr18:80247423-80247610 | Common:1; Rare:48 | ||||
| chr19:344775-344939 | Common:3; Rare:54 | ||||
| chr19:409106-409329 | Common:2; Rare:79 | ||||
| chr19:488979-489196 | Common:7; Rare:71 | ||||
| chr19:571231-571314 | Rare:18 | ||||
| chr19:571458-571552 | Common:2; Rare:32 | ||||
| chr19:572387-572719 | Common:1; Rare:174 | ||||
| chr19:582549-582822 | Common:6; Rare:107 | ||||
| chr19:633466-633764 | Common:8; Rare:137 | ||||
| chr19:639567-639930 | Common:5; Rare:130 | ||||
| chr19:663108-663386 | Common:3; Rare:107 | ||||
| chr19:680458-680760 | Common:2; Rare:104 | ||||
| chr19:797767-798041 | Common:4; Rare:164 |