Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:214280998-214281252 | Common:2; Rare:107 | ||||
chr1:214603040-214603317 | Common:3; Rare:74 | ||||
chr1:217631029-217631385 | Common:3; Rare:102 | ||||
chr1:219173713-219173902 | Common:1; Rare:86 | ||||
chr1:220046416-220046742 | Common:1; Rare:104 | ||||
chr1:220272412-220272654 | Rare:73; Clinvar:4 | ||||
chr1:221742065-221742325 | Common:1; Rare:75 | ||||
chr1:222589912-222589972 | Rare:10 | ||||
chr1:222644137-222644386 | Common:1; Rare:73 | ||||
chr1:222712459-222712864 | Common:3; Rare:145 | ||||
chr1:224114004-224114132 | Common:1; Rare:48 | ||||
chr1:224330128-224330418 | Common:6; Rare:83 | ||||
chr1:225427998-225428270 | Common:3; Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
chr1:225777716-225777895 | Common:3; Rare:53 | ||||
chr1:225924242-225924523 | Common:8; Rare:77 |