| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10711990-10712298 | Rare:99 | ||||
| chr19:10835558-10835905 | Common:2; Rare:99 | ||||
| chr19:10836196-10836693 | Common:3; Rare:135 | ||||
| chr19:10871595-10871877 | Common:8; Rare:101 | ||||
| chr19:10919362-10919640 | Common:1; Rare:41 | ||||
| chr19:10928517-10928885 | Common:2; Rare:122 | ||||
| chr19:10960706-10961167 | Common:3; Rare:166; Clinvar (benign):2 | ||||
| chr19:11089294-11089526 | Rare:42; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11155750-11156047 | Common:3; Rare:74 | ||||
| chr19:11197484-11197684 | Common:1; Rare:62 | ||||
| chr19:11339496-11339764 | Common:3; Rare:59 | ||||
| chr19:11361625-11361752 | Rare:26 | ||||
| chr19:11374462-11374740 | Common:1; Rare:83 | ||||
| chr19:11374882-11375246 | Common:1; Rare:118 | ||||
| chr19:11381160-11381444 | Common:1; Rare:92; Clinvar:1 |