Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89820908-89821253 | Common:1; Rare:103 | ||||
chr1:89821792-89821893 | Rare:31 | ||||
chr1:89994973-89995218 | Common:2; Rare:90 | ||||
chr1:91500718-91500910 | Common:2; Rare:63 | ||||
chr1:91501364-91501391 | Rare:9 | ||||
chr1:91886085-91886402 | Rare:120 | ||||
chr1:92298944-92299070 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079089-93079303 | Common:2; Rare:91 | ||||
chr1:93179608-93179966 | Common:2; Rare:68 | ||||
chr1:93180017-93180758 | Common:2; Rare:285 | ||||
chr1:93345698-93345962 | Common:4; Rare:95 | ||||
chr1:93447980-93448168 | Common:2; Rare:66 | ||||
chr1:93879144-93879274 | Common:1; Rare:44 | ||||
chr1:94237560-94237788 | Rare:85 | ||||
chr1:94418185-94418523 | Common:2; Rare:117 |