Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58006351-58006700 | Common:2; Rare:93 | ||||
chr17:58007214-58007520 | Common:1; Rare:121 | ||||
chr17:58219216-58219376 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):4 | ||||
chr17:58514571-58514760 | Rare:39 | ||||
chr17:59106685-59106970 | Common:2; Rare:95; Clinvar:5; Clinvar (benign):3 | ||||
chr17:59155012-59155502 | Common:2; Rare:124 | ||||
chr17:59155560-59155784 | Rare:62 | ||||
chr17:59619590-59620160 | Common:3; Rare:197 | ||||
chr17:59707370-59707744 | Common:4; Rare:102; Clinvar (benign):6 | ||||
chr17:59837635-59838089 | Common:1; Rare:69 | ||||
chr17:59838140-59838212 | Rare:7 | ||||
chr17:59892715-59893140 | Rare:113 | ||||
chr17:60078918-60078988 | Common:4; Rare:36 | ||||
chr17:60525900-60526332 | Common:2; Rare:154 | ||||
chr17:61399521-61399920 | Common:1; Rare:110 |