Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:127949675-127949947 | Common:1; Rare:55 | ||||
chr8:128176669-128177123 | Common:1; Rare:91 | ||||
chr8:128177437-128177458 | Rare:2 | ||||
chr8:132321485-132321725 | Rare:42 | ||||
chr8:133054742-133055032 | Rare:44 | ||||
chr8:133068651-133068820 | Common:1; Rare:47 | ||||
chr8:133072151-133072386 | Common:2; Rare:43 | ||||
chr8:133078054-133078242 | Common:3; Rare:28 | ||||
chr8:133242028-133242128 | Common:1; Rare:28; Clinvar:3; Clinvar (benign):2 | ||||
chr8:133294950-133295044 | Rare:23 | ||||
chr8:134831238-134831480 | Rare:56 | ||||
chr8:140597009-140597276 | Common:2; Rare:62 | ||||
chr8:142613225-142613243 | Rare:5 | ||||
chr8:143816743-143817012 | Common:1; Rare:81 | ||||
chr8:143929519-143929725 | Common:1; Rare:80; Clinvar:3; Clinvar (benign):3 |