Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1324607-1324910 | Common:3; Rare:148 | ||||
chr1:1658953-1659058 | Common:1; Rare:39 | ||||
chr1:1724286-1724631 | Common:5; Rare:121 | ||||
chr1:2391540-2391868 | Common:2; Rare:120 | ||||
chr1:3900219-3900589 | Common:12; Rare:141 | ||||
chr1:6208680-6208886 | Common:1; Rare:58 | ||||
chr1:6491665-6491804 | Rare:16 | ||||
chr1:6701790-6701964 | Rare:55 | ||||
chr1:7771174-7771372 | Common:3; Rare:88 | ||||
chr1:7961416-7961757 | Common:4; Rare:123; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878597-8878874 | Rare:149 | ||||
chr1:9943318-9943488 | Common:2; Rare:38 | ||||
chr1:11262515-11262828 | Common:1; Rare:91 | ||||
chr1:11934549-11934765 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):1 | ||||
chr1:13749193-13749439 | Common:2; Rare:85 |