Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:122152194-122152390 | Common:2; Rare:82 | ||||
chr4:122732432-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
chr4:122922923-122923145 | Common:2; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr4:127782267-127782332 | Rare:18 | ||||
chr4:127880797-127880939 | Rare:46 | ||||
chr4:128060985-128061329 | Common:1; Rare:124 | ||||
chr4:128811143-128811313 | Rare:35 | ||||
chr4:129093468-129093742 | Common:1; Rare:81 | ||||
chr4:133149111-133149294 | Common:2; Rare:52 | ||||
chr4:139177192-139177373 | Rare:49 | ||||
chr4:139301291-139301568 | Common:4; Rare:88 | ||||
chr4:139453674-139454190 | Common:5; Rare:140; Clinvar:10; Clinvar (benign):4 | ||||
chr4:140373380-140373701 | Common:2; Rare:129 | ||||
chr4:140523929-140524222 | Common:2; Rare:90 | ||||
chr4:141220770-141220986 | Rare:74 |