| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51366271-51366551 | Common:5; Rare:85; Clinvar (benign):2 | ||||
| chr19:51751866-51751976 | Common:2; Rare:23 | ||||
| chr19:52028345-52028456 | Common:3; Rare:21 | ||||
| chr19:52269431-52269603 | Common:1; Rare:60 | ||||
| chr19:52397683-52397889 | Common:5; Rare:60 | ||||
| chr19:52735024-52735161 | Common:2; Rare:38 | ||||
| chr19:52786733-52786904 | Common:8; Rare:48 | ||||
| chr19:52897674-52897932 | Rare:70 | ||||
| chr19:52962861-52963082 | Common:3; Rare:70 | ||||
| chr19:53254845-53255019 | Rare:57 | ||||
| chr19:53395025-53395161 | Common:4; Rare:43 | ||||
| chr19:53867583-53867943 | Common:1; Rare:88 | ||||
| chr19:54102684-54102881 | Common:3; Rare:52 | ||||
| chr19:54115635-54115792 | Common:1; Rare:34; Clinvar:4 | ||||
| chr19:54159673-54160005 | Rare:117 |