Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:70255463-70255653 | Common:5; Rare:60 | ||||
chr14:70293583-70293821 | Common:1; Rare:46 | ||||
chr14:81219339-81219504 | Rare:37 | ||||
chr14:102009712-102009925 | Common:2; Rare:44; Clinvar (benign):2 | ||||
chr14:102010071-102010312 | Common:1; Rare:66; Clinvar (benign):5 | ||||
chr14:102411571-102411641 | Rare:8 | ||||
chr14:103561154-103561380 | Common:2; Rare:52 | ||||
chr15:23303503-23303786 | Common:1; Rare:29 | ||||
chr15:24859038-24859180 | Common:1; Rare:25 | ||||
chr15:24919339-24919693 | Common:5; Rare:74 | ||||
chr15:24956296-24956456 | Common:3; Rare:59 | ||||
chr15:24993868-24994042 | Common:1; Rare:42 | ||||
chr15:25050854-25050941 | Common:1; Rare:25 | ||||
chr15:25089729-25089972 | Common:1; Rare:55 | ||||
chr15:25119119-25119254 | Rare:29 |