Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:106316191-106316597 | Common:5; Rare:131 | ||||
chr4:107720183-107720499 | Common:7; Rare:127 | ||||
chr4:107989689-107989865 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):3 | ||||
chr4:108620393-108620654 | Common:6; Rare:132 | ||||
chr4:109560157-109560389 | Rare:72 | ||||
chr4:109703401-109703606 | Common:1; Rare:65 | ||||
chr4:112636875-112637197 | Common:1; Rare:88 | ||||
chr4:113978988-113979291 | Common:4; Rare:50 | ||||
chr4:113979582-113979698 | Common:1; Rare:27 | ||||
chr4:119212408-119212730 | Common:2; Rare:98 | ||||
chr4:120066769-120066944 | Common:3; Rare:52 | ||||
chr4:122732436-122732690 | Rare:73 | ||||
chr4:122922902-122923145 | Common:2; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr4:127632843-127632960 | Rare:27 | ||||
chr4:127880765-127880939 | Rare:62 |