Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:57621713-57622079 | Common:3; Rare:127 | ||||
chr18:57803059-57803261 | Common:1; Rare:59; Clinvar (benign):1 | ||||
chr18:57803340-57803462 | Common:1; Rare:34 | ||||
chr18:59697345-59697732 | Common:1; Rare:125; Clinvar:1 | ||||
chr18:60372772-60372925 | Rare:30 | ||||
chr18:62186937-62187320 | Common:5; Rare:106 | ||||
chr18:62522762-62523062 | Common:4; Rare:102 | ||||
chr18:63367115-63367351 | Common:1; Rare:86 | ||||
chr18:63367543-63367666 | Common:3; Rare:42 | ||||
chr18:63422339-63422665 | Common:1; Rare:89 | ||||
chr18:68714977-68715271 | Common:6; Rare:128 | ||||
chr18:70205659-70205770 | Common:3; Rare:48; Clinvar (benign):2 | ||||
chr18:74148352-74148564 | Common:1; Rare:70 | ||||
chr18:74291862-74292208 | Common:2; Rare:97 | ||||
chr18:74496021-74496402 | Common:4; Rare:122 |