| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18323034-18323281 | Common:3; Rare:81 | ||||
| chr19:18539423-18539591 | Common:4; Rare:55 | ||||
| chr19:18557685-18557892 | Common:4; Rare:54 | ||||
| chr19:18571629-18571891 | Common:3; Rare:103 | ||||
| chr19:18683525-18683697 | Common:1; Rare:59 | ||||
| chr19:18919349-18919753 | Common:2; Rare:145 | ||||
| chr19:19033475-19033649 | Common:2; Rare:54 | ||||
| chr19:19033831-19033882 | Rare:11 | ||||
| chr19:19192128-19192268 | Common:1; Rare:44 | ||||
| chr19:19192614-19192984 | Common:2; Rare:88 | ||||
| chr19:19516157-19516302 | Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19865714-19865926 | Common:2; Rare:55 | ||||
| chr19:19900763-19900978 | Common:1; Rare:61 | ||||
| chr19:21082019-21082248 | Rare:50 | ||||
| chr19:21141731-21142100 | Common:1; Rare:94 |