| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38374489-38374817 | Rare:131 | ||||
| chr19:38930753-38930958 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:39391057-39391404 | Common:1; Rare:138 | ||||
| chr19:40348399-40348720 | Common:4; Rare:102 | ||||
| chr19:43754910-43755104 | Common:3; Rare:65 | ||||
| chr19:45507228-45507499 | Common:1; Rare:68 | ||||
| chr19:45692381-45692691 | Common:1; Rare:69 | ||||
| chr19:46600987-46601364 | Common:4; Rare:127 | ||||
| chr19:48619162-48619492 | Common:1; Rare:98 | ||||
| chr19:49665778-49666027 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
| chr19:54115630-54115787 | Common:1; Rare:35; Clinvar:4 | ||||
| chr19:54449049-54449220 | Common:2; Rare:48 | ||||
| chr2:677387-677557 | Rare:67 | ||||
| chr2:3558269-3558706 | Common:6; Rare:155 | ||||
| chr2:9423483-9423676 | Rare:57 |