Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:101347585-101347834 | Common:4; Rare:74 | ||||
chr4:102825751-102825891 | Rare:38 | ||||
chr4:102827120-102827405 | Common:1; Rare:104 | ||||
chr4:102827433-102827628 | Rare:69 | ||||
chr4:102827634-102828288 | Common:7; Rare:213 | ||||
chr4:102868836-102869063 | Common:2; Rare:77 | ||||
chr4:105708633-105708879 | Common:3; Rare:79 | ||||
chr4:106316191-106316593 | Common:5; Rare:128 | ||||
chr4:107720197-107720556 | Common:7; Rare:143 | ||||
chr4:107989690-107989907 | Common:5; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
chr4:108620473-108620640 | Common:4; Rare:87 | ||||
chr4:109560088-109560370 | Common:3; Rare:80 | ||||
chr4:109730037-109730218 | Common:3; Rare:40 | ||||
chr4:109815380-109815798 | Common:2; Rare:107 | ||||
chr4:110198520-110198678 | Rare:48 |