Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:87331858-87332104 | Rare:75 | ||||
chr1:88683943-88684452 | Common:4; Rare:138 | ||||
chr1:88684944-88685148 | Rare:56 | ||||
chr1:88833091-88833407 | Common:1; Rare:89 | ||||
chr1:88891501-88891757 | Common:1; Rare:107 | ||||
chr1:89632900-89633189 | Common:1; Rare:81 | ||||
chr1:89821745-89821858 | Rare:34 | ||||
chr1:89994981-89995269 | Common:2; Rare:115 | ||||
chr1:91886064-91886355 | Rare:119 | ||||
chr1:92298910-92299090 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92831972-92832112 | Common:1; Rare:79; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92833129-92833456 | Common:1; Rare:77; Clinvar (pathogenic):1 | ||||
chr1:93079040-93079325 | Common:4; Rare:122 | ||||
chr1:93179596-93180029 | Common:2; Rare:86 | ||||
chr1:93180055-93180262 | Rare:76 |