Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1742729-1743059 | Common:1; Rare:74 | ||||
chr17:1762606-1762881 | Common:4; Rare:60 | ||||
chr17:1829786-1830057 | Common:8; Rare:113 | ||||
chr17:2303468-2303631 | Rare:60 | ||||
chr17:2303774-2303987 | Common:2; Rare:76 | ||||
chr17:2336423-2336551 | Rare:50 | ||||
chr17:2593923-2593988 | Rare:15 | ||||
chr17:2701239-2701471 | Rare:85 | ||||
chr17:2711762-2712043 | Common:2; Rare:79 | ||||
chr17:3636219-3636540 | Common:4; Rare:97; Clinvar (benign):1 | ||||
chr17:3636635-3636798 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
chr17:3668533-3668828 | Common:3; Rare:117 | ||||
chr17:3723757-3723913 | Common:1; Rare:86 | ||||
chr17:4142987-4143258 | Rare:93 | ||||
chr17:4143597-4143735 | Common:4; Rare:79 |