Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49149367-49149501 | Rare:42 | ||||
chr19:49149621-49150023 | Common:1; Rare:89 | ||||
chr19:49157632-49157850 | Rare:66; Clinvar:1 | ||||
chr19:49451735-49451999 | Common:3; Rare:68 | ||||
chr19:49453094-49453300 | Common:1; Rare:65 | ||||
chr19:49453480-49453666 | Common:1; Rare:60 | ||||
chr19:49487284-49487644 | Common:5; Rare:129 | ||||
chr19:49496358-49496476 | Common:1; Rare:59 | ||||
chr19:49580534-49580680 | Rare:45 | ||||
chr19:49665584-49666020 | Common:6; Rare:199; Clinvar (pathogenic):1 | ||||
chr19:49690598-49690878 | Common:2; Rare:58 | ||||
chr19:49690881-49690915 | Rare:7 | ||||
chr19:49690950-49691211 | Common:2; Rare:59 | ||||
chr19:49691433-49691541 | Common:2; Rare:35 | ||||
chr19:49701385-49701465 | Rare:41 |