| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5790827-5790969 | Common:2; Rare:44 | ||||
| chr19:5791106-5791359 | Common:6; Rare:84 | ||||
| chr19:5903706-5903958 | Common:3; Rare:117; Clinvar:6; Clinvar (benign):4 | ||||
| chr19:5904000-5904277 | Common:4; Rare:71; Clinvar:1 | ||||
| chr19:5904321-5904400 | Common:1; Rare:22 | ||||
| chr19:5904585-5905059 | Common:5; Rare:143 | ||||
| chr19:5978021-5978480 | Common:3; Rare:179 | ||||
| chr19:6057273-6057491 | Common:1; Rare:42 | ||||
| chr19:6110447-6110941 | Common:6; Rare:135 | ||||
| chr19:6199465-6199913 | Common:14; Rare:144 | ||||
| chr19:6279541-6279673 | Common:1; Rare:36 | ||||
| chr19:6279889-6280290 | Common:4; Rare:119 | ||||
| chr19:6361439-6361616 | Common:1; Rare:59; Clinvar (benign):3 | ||||
| chr19:6361629-6361794 | Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:6372426-6372853 | Common:5; Rare:139 |