Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:23579247-23579407 | Common:2; Rare:50 | ||||
chr13:23889298-23889545 | Common:1; Rare:91 | ||||
chr13:24512732-24512861 | Common:3; Rare:38 | ||||
chr13:24922801-24923045 | Common:1; Rare:76; Clinvar:1 | ||||
chr13:25301401-25301692 | Common:1; Rare:103 | ||||
chr13:26221791-26221924 | Rare:34 | ||||
chr13:27251235-27251617 | Common:8; Rare:117 | ||||
chr13:27270692-27270865 | Rare:66 | ||||
chr13:27424507-27424740 | Common:3; Rare:76 | ||||
chr13:27450130-27450214 | Common:3; Rare:24 | ||||
chr13:27450381-27450685 | Common:4; Rare:114 | ||||
chr13:27620416-27620818 | Common:3; Rare:136 | ||||
chr13:28138145-28138234 | Common:1; Rare:25 | ||||
chr13:28659071-28659187 | Rare:49; Clinvar (pathogenic):1 | ||||
chr13:29428346-29428680 | Common:3; Rare:85 |