Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97445981-97446225 | Not yet | Rare:63 | 354 | ||
chr10:97498694-97498993 | Not yet | Common:2; Rare:86 | 310 | ||
chr10:98134536-98134688 | Not yet | Common:1; Rare:54 | 181 | ||
chr10:98134836-98134893 | Not yet | Rare:17 | 109 | ||
chr10:98446856-98446971 | Not yet | Rare:29 | 165 | ||
chr10:99430579-99430930 | Not yet | Common:4; Rare:81 | 353 | ||
chr10:99659264-99659536 | Not yet | Common:1; Rare:67 | 321 | ||
chr10:99732070-99732331 | Not yet | Rare:97; Clinvar:4; Clinvar (benign):1 | 271 | ||
chr10:100185895-100186184 | Not yet | Rare:108 | 272 | ||
chr10:100229553-100229689 | Not yet | Rare:49 | 213 | ||
chr10:100286603-100286751 | Not yet | Common:5; Rare:84 | 177 | ||
chr10:100346921-100347459 | Not yet | Common:3; Rare:124 | 425 | ||
chr10:100529823-100530010 | Not yet | Common:1; Rare:52 | 267 | ||
chr10:100912667-100913026 | Not yet | Common:1; Rare:106 | 396 | ||
chr10:100987210-100987584 | Not yet | Common:1; Rare:136; Clinvar:1; Clinvar (benign):1 | 322 |