Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:118735345-118735418 | Common:1; Rare:6 | ||||
chr4:118778371-118778457 | Common:1; Rare:14 | ||||
chr4:118781226-118781433 | Common:1; Rare:34 | ||||
chr4:118815025-118815716 | Common:8; Rare:191; Clinvar (benign):1 | ||||
chr4:119266286-119266344 | Rare:12 | ||||
chr4:119454600-119454904 | Common:14; Rare:101 | ||||
chr4:119498550-119498890 | Common:2; Rare:78 | ||||
chr4:119499289-119499380 | Rare:15 | ||||
chr4:119500694-119500910 | Common:3; Rare:47 | ||||
chr4:119504522-119504633 | Common:1; Rare:31 | ||||
chr4:119511428-119511560 | Rare:19 | ||||
chr4:119516991-119517071 | Common:2; Rare:10 | ||||
chr4:119525385-119525584 | Common:2; Rare:43 | ||||
chr4:119537247-119537447 | Rare:35 | ||||
chr4:119544579-119544657 | Rare:17 |