| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42325385-42325687 | Rare:79 | ||||
| chr19:43504093-43504384 | Common:7; Rare:91 | ||||
| chr19:43527180-43527276 | Common:4; Rare:45; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575448-43575837 | Common:3; Rare:103 | ||||
| chr19:43580483-43580643 | Common:3; Rare:25 | ||||
| chr19:43596106-43596472 | Common:2; Rare:109 | ||||
| chr19:43619563-43620116 | Common:4; Rare:162 | ||||
| chr19:43639768-43639930 | Common:1; Rare:58 | ||||
| chr19:43670155-43670306 | Common:2; Rare:30 | ||||
| chr19:43754855-43755094 | Common:3; Rare:98 | ||||
| chr19:43827203-43827433 | Common:2; Rare:48 | ||||
| chr19:43901761-43901925 | Common:3; Rare:35 | ||||
| chr19:43935231-43935306 | Common:2; Rare:25 | ||||
| chr19:43951119-43951308 | Common:1; Rare:50 | ||||
| chr19:44002815-44002993 | Common:4; Rare:45 |