| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44813282-44813718 | Common:10; Rare:291; Clinvar (pathogenic):4 | ||||
| chr19:44845970-44846423 | Common:8; Rare:216 | ||||
| chr19:44890918-44891355 | Common:8; Rare:290 | ||||
| chr19:44905561-44905907 | Common:4; Rare:195; Clinvar:2 | ||||
| chr19:44914094-44914356 | Common:4; Rare:93 | ||||
| chr19:44914473-44914945 | Common:3; Rare:186 | ||||
| chr19:44954780-44955090 | Common:5; Rare:126 | ||||
| chr19:44955237-44955427 | Common:4; Rare:115 | ||||
| chr19:45038937-45039117 | Rare:117 | ||||
| chr19:45076438-45076585 | Rare:89 | ||||
| chr19:45079130-45079410 | Common:1; Rare:119 | ||||
| chr19:45092827-45093268 | Common:7; Rare:260 | ||||
| chr19:45178165-45178564 | Common:5; Rare:189 | ||||
| chr19:45251169-45251319 | Common:2; Rare:80 | ||||
| chr19:45370519-45370834 | Common:4; Rare:180; Clinvar:2 |