| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48810849-48810994 | Rare:39 | ||||
| chr19:48810999-48811124 | Rare:43 | ||||
| chr19:48835818-48835958 | Common:1; Rare:44 | ||||
| chr19:48872210-48872455 | Common:2; Rare:85 | ||||
| chr19:48900157-48900407 | Common:1; Rare:79 | ||||
| chr19:48918776-48919073 | Common:3; Rare:106 | ||||
| chr19:48933588-48933709 | Common:3; Rare:39 | ||||
| chr19:48954593-48954931 | Common:1; Rare:119 | ||||
| chr19:48993188-48993915 | Common:9; Rare:258; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49064973-49065268 | Rare:59 | ||||
| chr19:49085106-49085492 | Common:3; Rare:153 | ||||
| chr19:49114122-49114580 | Common:6; Rare:123 | ||||
| chr19:49153944-49154778 | Common:14; Rare:337; Clinvar (benign):1 | ||||
| chr19:49155353-49155534 | Rare:33 | ||||
| chr19:49157580-49157852 | Common:2; Rare:89; Clinvar:1 |