| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38912163-38912275 | Rare:35 | ||||
| chr19:38930726-38931005 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975718-38975840 | Common:1; Rare:25 | ||||
| chr19:39125578-39125805 | Rare:53 | ||||
| chr19:39390845-39390925 | Rare:33 | ||||
| chr19:39390981-39391425 | Common:1; Rare:170 | ||||
| chr19:39406706-39406847 | Rare:53 | ||||
| chr19:39412368-39412724 | Common:3; Rare:123 | ||||
| chr19:39435850-39436188 | Common:8; Rare:130 | ||||
| chr19:39445470-39445822 | Common:2; Rare:97 | ||||
| chr19:39480602-39480937 | Common:3; Rare:162; Clinvar (pathogenic):1 | ||||
| chr19:39498730-39498964 | Common:2; Rare:64; Clinvar:1 | ||||
| chr19:39846307-39846539 | Common:1; Rare:112 | ||||
| chr19:39970834-39971223 | Common:5; Rare:113 | ||||
| chr19:39996903-39997113 | Common:5; Rare:63 |