Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61324024-61324306 | Common:1; Rare:39 | ||||
chr1:61700929-61701302 | Common:2; Rare:59 | ||||
chr1:61869021-61869094 | Common:1; Rare:10 | ||||
chr1:61962076-61962380 | Common:1; Rare:48 | ||||
chr1:62041545-62041742 | Rare:35 | ||||
chr1:62115947-62116049 | Rare:14 | ||||
chr1:62625300-62625597 | Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
chr1:62648253-62648538 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
chr1:62711386-62711646 | Rare:34 | ||||
chr1:63424925-63425190 | Common:2; Rare:39 | ||||
chr1:63659420-63659650 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
chr1:63797821-63797849 | Rare:2 | ||||
chr1:63833589-63833655 | Rare:9 | ||||
chr1:64065436-64065633 | Rare:33 | ||||
chr1:65212577-65212634 | Rare:9 |