Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:241637561-241637704 | Common:1; Rare:79 | ||||
chr2:241686749-241687139 | Common:4; Rare:124 | ||||
chr20:1118449-1118737 | Common:5; Rare:92 | ||||
chr20:2652434-2652671 | Common:8; Rare:88 | ||||
chr20:2840627-2840775 | Common:1; Rare:59 | ||||
chr20:2841081-2841235 | Common:2; Rare:31 | ||||
chr20:3209433-3209551 | Common:1; Rare:41 | ||||
chr20:3767719-3768067 | Common:5; Rare:109 | ||||
chr20:3796142-3796549 | Common:4; Rare:94 | ||||
chr20:3820466-3820606 | Rare:54 | ||||
chr20:3846727-3846893 | Rare:49 | ||||
chr20:3889161-3889379 | Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
chr20:5950300-5950720 | Common:8; Rare:127 | ||||
chr20:6006468-6006529 | Rare:11 | ||||
chr20:13784884-13785071 | Common:2; Rare:81; Clinvar (benign):3 |