Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:72728290-72728587 | Rare:50 | ||||
chr10:72742489-72742732 | Rare:38 | ||||
chr10:72805024-72805072 | Rare:12 | ||||
chr10:72849303-72849447 | Rare:28 | ||||
chr10:73004011-73004161 | Common:1; Rare:20 | ||||
chr10:73038498-73038610 | Rare:10 | ||||
chr10:73095415-73095515 | Rare:10 | ||||
chr10:73126102-73126224 | Common:1; Rare:18 | ||||
chr10:73156387-73156652 | Common:1; Rare:67 | ||||
chr10:73215477-73215499 | Rare:1 | ||||
chr10:73246687-73246996 | Rare:119 | ||||
chr10:73247025-73247418 | Common:2; Rare:184 | ||||
chr10:73250981-73251099 | Rare:37; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr10:73451346-73451603 | Rare:49 | ||||
chr10:73451610-73451732 | Rare:16 |