Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:30682247-30682305 | Common:1; Rare:9 | ||||
chr6:31400590-31400721 | Common:5; Rare:29 | ||||
chr6:32049550-32049809 | Common:6; Rare:71; Clinvar (benign):2 | ||||
chr6:32894561-32894782 | Common:9; Rare:60 | ||||
chr6:35490150-35490420 | Common:1; Rare:83 | ||||
chr6:35590927-35591080 | Rare:31 | ||||
chr6:35687573-35687762 | Rare:34 | ||||
chr6:36479506-36479596 | Common:1; Rare:26 | ||||
chr6:36680156-36680165 | |||||
chr6:39819806-39820003 | Common:4; Rare:44 | ||||
chr6:39821961-39822116 | Rare:37 | ||||
chr6:39896881-39897269 | Common:3; Rare:102 | ||||
chr6:42929729-42929774 | Rare:25 | ||||
chr6:42956693-42956931 | Common:5; Rare:47 | ||||
chr6:43172265-43172431 | Common:1; Rare:30 |