Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23338145-23338393 | Common:4; Rare:40 | ||||
chr1:23340334-23340630 | Common:1; Rare:44 | ||||
chr1:23344186-23344547 | Common:2; Rare:125 | ||||
chr1:23368284-23368508 | Common:1; Rare:61 | ||||
chr1:23368852-23369019 | Common:1; Rare:56 | ||||
chr1:23369171-23369270 | Common:2; Rare:33 | ||||
chr1:23369752-23370011 | Rare:45 | ||||
chr1:23558894-23559676 | Common:8; Rare:361 | ||||
chr1:23559704-23559762 | Rare:21 | ||||
chr1:23559831-23560103 | Common:1; Rare:81 | ||||
chr1:23581276-23581518 | Rare:65 | ||||
chr1:23692179-23692366 | Rare:55 | ||||
chr1:23692384-23692902 | Common:6; Rare:141; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23778269-23778488 | Common:9; Rare:114 | ||||
chr1:23791066-23791366 | Common:1; Rare:74 |