Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:141728618-141728775 | Common:2; Rare:37 | ||||
chr8:141730360-141730470 | Common:1; Rare:25 | ||||
chr8:141730561-141730592 | Rare:4 | ||||
chr8:141731077-141731271 | Rare:37 | ||||
chr8:142876473-142877222 | Common:6; Rare:251; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr8:142878497-142878530 | Rare:8 | ||||
chr8:142878907-142879254 | Common:3; Rare:147; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr8:142924705-142924889 | Rare:38 | ||||
chr8:142952149-142952272 | Common:1; Rare:15 | ||||
chr8:143039206-143039476 | Common:5; Rare:55 | ||||
chr8:143281625-143281815 | Common:3; Rare:48 | ||||
chr8:145002821-145003047 | Common:2; Rare:83 | ||||
chr8:145004829-145004856 | Rare:7 | ||||
chr8:145021390-145021541 | Common:12; Rare:70 | ||||
chr8:145027564-145027779 | Common:3; Rare:56 |