| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10701560-10702035 | Common:2; Rare:197 | ||||
| chr19:10717259-10718277 | Common:3; Rare:450; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:10718389-10718595 | Common:3; Rare:98; Clinvar:1 | ||||
| chr19:10835460-10836180 | Common:6; Rare:521 | ||||
| chr19:10836167-10836709 | Common:8; Rare:355 | ||||
| chr19:10870817-10871122 | Common:2; Rare:93 | ||||
| chr19:10871052-10871730 | Common:28; Rare:723 | ||||
| chr19:10928454-10928919 | Common:7; Rare:412 | ||||
| chr19:10960577-10961199 | Common:20; Rare:532; Clinvar (benign):4 | ||||
| chr19:10961202-10961327 | Rare:46 | ||||
| chr19:10983851-10984480 | Common:1; Rare:294; Clinvar:56; Clinvar (benign):32 | ||||
| chr19:11089238-11089616 | Rare:203; Clinvar:46; Clinvar (benign):2; Clinvar (pathogenic):10 | ||||
| chr19:11090220-11090697 | Common:6; Rare:322 | ||||
| chr19:11155689-11156086 | Common:9; Rare:280 | ||||
| chr19:11196711-11197111 | Common:3; Rare:120 |