| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10106495-10106627 | Common:1; Rare:53 | ||||
| chr19:10119804-10120050 | Common:1; Rare:94 | ||||
| chr19:10194559-10194730 | Common:1; Rare:40 | ||||
| chr19:10194828-10195239 | Common:2; Rare:168; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:10230913-10231040 | Common:2; Rare:35 | ||||
| chr19:10231097-10231458 | Common:1; Rare:78 | ||||
| chr19:10251924-10252028 | Common:1; Rare:26 | ||||
| chr19:10252099-10252285 | Common:2; Rare:82 | ||||
| chr19:10252384-10252465 | Rare:24 | ||||
| chr19:10286978-10287242 | Common:1; Rare:99 | ||||
| chr19:10289519-10289715 | Common:2; Rare:46 | ||||
| chr19:10315463-10315505 | Rare:16 | ||||
| chr19:10315714-10316098 | Common:7; Rare:175; Clinvar (benign):13 | ||||
| chr19:10332858-10333340 | Rare:123 | ||||
| chr19:10333354-10333796 | Common:1; Rare:151 |