Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38005495-38005766 | Common:1; Rare:68 | ||||
chr1:38859681-38860033 | Rare:138 | ||||
chr1:38873301-38873564 | Common:3; Rare:93 | ||||
chr1:39025978-39026136 | Rare:23 | ||||
chr1:39026216-39026398 | Common:1; Rare:47 | ||||
chr1:39215056-39215288 | Rare:40 | ||||
chr1:39639611-39639828 | Rare:86 | ||||
chr1:39954974-39955215 | Common:1; Rare:63 | ||||
chr1:40039923-40040255 | Common:3; Rare:74 | ||||
chr1:40040438-40040806 | Common:3; Rare:112 | ||||
chr1:40161272-40161478 | Rare:75 | ||||
chr1:40257898-40258332 | Common:4; Rare:127; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40344563-40344850 | Rare:45 | ||||
chr1:40373505-40373829 | Common:1; Rare:78 | ||||
chr1:40373927-40374141 | Rare:49 |