Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114716733-114716860 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):1 | ||||
chr1:117060280-117060341 | Common:2; Rare:22 | ||||
chr1:117929585-117929811 | Common:3; Rare:66 | ||||
chr1:119140634-119140767 | Rare:42 | ||||
chr1:145823937-145824238 | Rare:106 | ||||
chr1:145918700-145919022 | Common:2; Rare:69 | ||||
chr1:145927433-145927644 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:145964593-145964731 | Rare:28 | ||||
chr1:145996567-145996848 | Common:1; Rare:106 | ||||
chr1:147172457-147172714 | Common:1; Rare:63 | ||||
chr1:148952264-148952617 | Common:5; Rare:102 | ||||
chr1:149812349-149812560 | Rare:68 | ||||
chr1:149842748-149842964 | Rare:3 | ||||
chr1:149850846-149851063 | Rare:1 | ||||
chr1:149886632-149887036 | Common:3; Rare:153 |