Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:149345327-149345607 | Common:1; Rare:105 | ||||
chr5:149550041-149550259 | Rare:43 | ||||
chr5:149550276-149550432 | Rare:28 | ||||
chr5:149550809-149551124 | Rare:80 | ||||
chr5:149551328-149551656 | Rare:78 | ||||
chr5:149960569-149960859 | Rare:110; Clinvar:7 | ||||
chr5:150264928-150264964 | Rare:12 | ||||
chr5:150289687-150289882 | Common:1; Rare:52 | ||||
chr5:150290065-150290283 | Common:1; Rare:45 | ||||
chr5:150357433-150357749 | Rare:104; Clinvar:2; Clinvar (benign):4 | ||||
chr5:150449645-150449803 | Common:4; Rare:53 | ||||
chr5:150485710-150485910 | Common:1; Rare:49 | ||||
chr5:150700476-150700684 | Common:2; Rare:72 | ||||
chr5:150700975-150701235 | Common:2; Rare:102 | ||||
chr5:150758971-150759154 | Common:3; Rare:75 |