Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:29390543-29390875 | Rare:86 | ||||
chr17:29566268-29566332 | Rare:27 | ||||
chr17:29566983-29567285 | Rare:75 | ||||
chr17:29567897-29568116 | Common:1; Rare:40 | ||||
chr17:29568471-29568772 | Common:4; Rare:109 | ||||
chr17:29761286-29761577 | Common:4; Rare:108 | ||||
chr17:29929609-29929918 | Common:1; Rare:78 | ||||
chr17:29930165-29930252 | Rare:28 | ||||
chr17:30291892-30292161 | Common:1; Rare:94 | ||||
chr17:30824635-30824835 | Common:3; Rare:86 | ||||
chr17:30906200-30906346 | Common:1; Rare:44 | ||||
chr17:30970925-30971067 | Common:1; Rare:54 | ||||
chr17:31095365-31095594 | Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
chr17:31273614-31273670 | Rare:4 | ||||
chr17:31321604-31321682 | Rare:10 |