| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3180180-3180282 | Common:1; Rare:16 | ||||
| chr19:3977213-3977612 | Common:4; Rare:130; Clinvar (benign):8 | ||||
| chr19:4064795-4065044 | Common:1; Rare:74 | ||||
| chr19:4362379-4362661 | Rare:109 | ||||
| chr19:4519052-4519177 | Rare:32 | ||||
| chr19:4916750-4916869 | Rare:36 | ||||
| chr19:5221121-5221408 | Common:2; Rare:74 | ||||
| chr19:6414304-6414362 | Rare:28 | ||||
| chr19:7137881-7138045 | Common:4; Rare:29 | ||||
| chr19:7198044-7198294 | Common:4; Rare:78 | ||||
| chr19:7378855-7379129 | Common:2; Rare:57 | ||||
| chr19:7458416-7458580 | Rare:50 | ||||
| chr19:7523384-7523726 | Common:1; Rare:67 | ||||
| chr19:8500238-8500381 | Common:3; Rare:29 | ||||
| chr19:8522379-8522723 | Common:1; Rare:130; Clinvar (benign):1 |