| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50668451-50668851 | Common:2; Rare:98 | ||||
| chr19:50723115-50723515 | Common:7; Rare:232 | ||||
| chr19:50723561-50724577 | Rare:457 | ||||
| chr19:50803082-50803482 | Rare:113 | ||||
| chr19:50803887-50805243 | Common:103; Rare:1800 | ||||
| chr19:50820680-50821320 | Common:3; Rare:531 | ||||
| chr19:50823330-50823730 | Common:5; Rare:176 | ||||
| chr19:50870252-50870810 | Common:29; Rare:488 | ||||
| chr19:50909339-50909739 | Common:11; Rare:247; Clinvar (benign):3 | ||||
| chr19:51000991-51001391 | Common:5; Rare:152 | ||||
| chr19:51002618-51003025 | Common:10; Rare:188 | ||||
| chr19:51064740-51065230 | Common:10; Rare:289 | ||||
| chr19:51107710-51108950 | Common:26; Rare:784 | ||||
| chr19:51224354-51224754 | Common:1; Rare:87 | ||||
| chr19:51224971-51225371 | Common:5; Rare:305 |