Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71377434-71377586 | Common:4; Rare:37 | ||||
chr10:71834342-71834901 | Common:11; Rare:234; Clinvar:6; Clinvar (benign):8 | ||||
chr10:71860305-71860901 | Common:3; Rare:150 | ||||
chr10:71868290-71868630 | Common:4; Rare:101 | ||||
chr10:71888450-71888990 | Common:4; Rare:118 | ||||
chr10:71889083-71889220 | Common:3; Rare:27 | ||||
chr10:71965150-71965500 | Common:2; Rare:113 | ||||
chr10:72097700-72098080 | Common:2; Rare:106 | ||||
chr10:72243950-72244520 | Common:1; Rare:177 | ||||
chr10:72245039-72245237 | Rare:39 | ||||
chr10:72255040-72255492 | Common:1; Rare:152 | ||||
chr10:72259618-72260018 | Common:6; Rare:89 | ||||
chr10:72260422-72260644 | Rare:42 | ||||
chr10:72260685-72261033 | Common:1; Rare:132 | ||||
chr10:72263710-72263889 | Common:4; Rare:54 |