Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:143018406-143018582 | Common:1; Rare:51 | ||||
chr8:143558247-143558402 | Common:1; Rare:60 | ||||
chr8:143829310-143829482 | Rare:63 | ||||
chr8:144078512-144078722 | Common:1; Rare:64 | ||||
chr8:144082516-144082670 | Common:2; Rare:54 | ||||
chr9:26947159-26947216 | Rare:19 | ||||
chr9:33025090-33025357 | Common:7; Rare:116 | ||||
chr9:34048880-34048973 | Rare:37 | ||||
chr9:34329228-34329589 | Rare:107 | ||||
chr9:35657996-35658318 | Common:5; Rare:245; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
chr9:35732103-35732320 | Rare:62 | ||||
chr9:35732373-35732704 | Common:3; Rare:84 | ||||
chr9:35814983-35815293 | Rare:79 | ||||
chr9:69759942-69760119 | Common:2; Rare:85 | ||||
chr9:75088144-75088563 | Common:3; Rare:149 |