Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:76700417-76700610 | Rare:33 | ||||
chr8:79120353-79120526 | Common:2; Rare:36 | ||||
chr8:89535616-89535802 | Common:7; Rare:77 | ||||
chr8:126423055-126423246 | Rare:32 | ||||
chr8:127312007-127312182 | Common:1; Rare:45 | ||||
chr8:143281628-143281817 | Common:3; Rare:45 | ||||
chr8:145002858-145002948 | Rare:23 | ||||
chr9:14993151-14993330 | Common:5; Rare:76 | ||||
chr9:32550839-32551198 | Common:1; Rare:142; Clinvar:2; Clinvar (benign):2 | ||||
chr9:37079802-37079994 | Common:4; Rare:67 | ||||
chr9:39464494-39464657 | Rare:37 | ||||
chr9:39809154-39809400 | Common:2; Rare:16 | ||||
chr9:40991963-40992351 | Common:7; Rare:30 | ||||
chr9:41358819-41358904 | Common:1; Rare:28 | ||||
chr9:83219214-83219351 | Common:2; Rare:35 |