Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:121801165-121801411 | Common:3; Rare:88 | ||||
chr4:122152225-122152517 | Common:2; Rare:112 | ||||
chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
chr4:122922963-122923145 | Common:2; Rare:64; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr4:123396654-123396888 | Rare:58 | ||||
chr4:123399328-123399653 | Common:1; Rare:98 | ||||
chr4:127880797-127880929 | Rare:45 | ||||
chr4:128287773-128288022 | Common:3; Rare:96 | ||||
chr4:128811145-128811317 | Rare:36 | ||||
chr4:129093458-129093741 | Common:1; Rare:83 | ||||
chr4:133149099-133149325 | Common:2; Rare:69 | ||||
chr4:137532447-137532649 | Rare:31 | ||||
chr4:139301301-139301574 | Common:3; Rare:86 | ||||
chr4:139302463-139302484 | Rare:5 | ||||
chr4:139453694-139454225 | Common:5; Rare:151; Clinvar:10; Clinvar (benign):4 |