Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9996962-9997321 | Common:2; Rare:93 | ||||
chr1:10032751-10032991 | Rare:66 | ||||
chr1:10398797-10399103 | Common:2; Rare:117 | ||||
chr1:11099761-11099939 | Common:3; Rare:74 | ||||
chr1:11262493-11262836 | Common:2; Rare:101 | ||||
chr1:11654731-11654926 | Common:4; Rare:56 | ||||
chr1:11691766-11691945 | Rare:35 | ||||
chr1:11736096-11736187 | Common:2; Rare:34 | ||||
chr1:11805900-11806265 | Common:2; Rare:100; Clinvar:1 | ||||
chr1:11934509-11934754 | Common:3; Rare:81; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980104-11980462 | Common:6; Rare:113; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12617595-12617883 | Common:5; Rare:30 | ||||
chr1:12618132-12618497 | Common:3; Rare:75 | ||||
chr1:13700069-13700279 | Common:1; Rare:63 | ||||
chr1:15526578-15526913 | Common:2; Rare:107 |