| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50384036-50384380 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476469-50476542 | Rare:34 | ||||
| chr19:50511137-50511399 | Common:1; Rare:87 | ||||
| chr19:51366322-51366551 | Common:5; Rare:65; Clinvar (benign):2 | ||||
| chr19:52008171-52008290 | Rare:35 | ||||
| chr19:52028325-52028451 | Common:3; Rare:32 | ||||
| chr19:52962861-52963044 | Common:3; Rare:58 | ||||
| chr19:54115271-54115382 | Rare:28 | ||||
| chr19:54115615-54115797 | Common:2; Rare:46; Clinvar:5 | ||||
| chr19:54159682-54160075 | Rare:135 | ||||
| chr19:54200723-54200875 | Common:2; Rare:56 | ||||
| chr19:54449012-54449219 | Common:3; Rare:56 | ||||
| chr19:55258464-55258709 | Common:4; Rare:90 | ||||
| chr19:55339596-55339909 | Common:1; Rare:86 | ||||
| chr19:55370458-55370581 | Rare:20 |