| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18919344-18919744 | Common:2; Rare:141 | ||||
| chr19:19033482-19033658 | Common:2; Rare:54 | ||||
| chr19:19033799-19033922 | Common:1; Rare:35 | ||||
| chr19:19192115-19192212 | Common:1; Rare:35 | ||||
| chr19:19192624-19193015 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr19:19320483-19320853 | Common:4; Rare:131 | ||||
| chr19:19516167-19516306 | Rare:82; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19900795-19900998 | Common:1; Rare:52 | ||||
| chr19:20039231-20039309 | Common:1; Rare:18 | ||||
| chr19:20923121-20923288 | Rare:43 | ||||
| chr19:21141871-21142085 | Rare:58 | ||||
| chr19:29212904-29213245 | Common:3; Rare:93 | ||||
| chr19:29606207-29606320 | Rare:40 | ||||
| chr19:29665241-29665512 | Common:4; Rare:98 | ||||
| chr19:29715047-29715297 | Common:1; Rare:89 |