Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:106316177-106316625 | Common:5; Rare:144 | ||||
chr4:107720164-107720509 | Common:7; Rare:140 | ||||
chr4:107989742-107989925 | Common:4; Rare:89; Clinvar:3; Clinvar (benign):4 | ||||
chr4:108168735-108168793 | Rare:12 | ||||
chr4:108620391-108620658 | Common:6; Rare:134 | ||||
chr4:109433789-109433978 | Common:1; Rare:62 | ||||
chr4:109560089-109560312 | Common:3; Rare:64 | ||||
chr4:112232123-112232276 | Common:1; Rare:66 | ||||
chr4:112285757-112285970 | Rare:67 | ||||
chr4:112636872-112637197 | Common:1; Rare:89 | ||||
chr4:112818030-112818127 | Rare:8 | ||||
chr4:118685318-118685566 | Common:2; Rare:71 | ||||
chr4:118836063-118836259 | Common:1; Rare:45 | ||||
chr4:119212365-119212749 | Common:4; Rare:117 | ||||
chr4:119300528-119300874 | Common:1; Rare:163 |