Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:22933807-22933867 | Common:1; Rare:23 | ||||
chr18:23872688-23873042 | Rare:87 | ||||
chr18:32092388-32092694 | Common:4; Rare:135 | ||||
chr18:35290199-35290377 | Common:2; Rare:66 | ||||
chr18:35972449-35972713 | Common:4; Rare:81 | ||||
chr18:36828763-36829131 | Common:3; Rare:134 | ||||
chr18:46098239-46098538 | Common:11; Rare:87; Clinvar (benign):5 | ||||
chr18:46104135-46104396 | Common:3; Rare:74; Clinvar (benign):1 | ||||
chr18:49460631-49460832 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr18:49561879-49562086 | Rare:53 | ||||
chr18:49813839-49814031 | Common:1; Rare:81 | ||||
chr18:62186987-62187313 | Common:5; Rare:93 | ||||
chr18:63422392-63422677 | Common:2; Rare:76 | ||||
chr18:63476631-63477027 | Common:6; Rare:91 | ||||
chr18:68715058-68715255 | Common:3; Rare:90 |