Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:12307929-12308297 | Common:6; Rare:139 | ||||
chr18:12657972-12658216 | Common:6; Rare:95 | ||||
chr18:12702665-12703110 | Common:3; Rare:178 | ||||
chr18:12947674-12948094 | Common:3; Rare:121 | ||||
chr18:13726509-13726720 | Common:3; Rare:81 | ||||
chr18:21600650-21600856 | Rare:49 | ||||
chr18:22933242-22933426 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
chr18:22933691-22933868 | Common:2; Rare:72 | ||||
chr18:23453172-23453359 | Rare:65 | ||||
chr18:23586426-23586537 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
chr18:24397801-24398019 | Common:2; Rare:92 | ||||
chr18:24426620-24426767 | Common:3; Rare:61 | ||||
chr18:35041250-35041440 | Common:1; Rare:67 | ||||
chr18:35240917-35241094 | Common:2; Rare:66 | ||||
chr18:35290193-35290384 | Common:2; Rare:68 |