Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86396259-86396413 | Common:3; Rare:37 | ||||
chr1:86704708-86704872 | Common:2; Rare:61 | ||||
chr1:88683980-88684337 | Common:3; Rare:105 | ||||
chr1:89065198-89065472 | Common:2; Rare:40 | ||||
chr1:89198851-89199001 | Rare:22 | ||||
chr1:89843339-89843680 | Common:3; Rare:132 | ||||
chr1:89994981-89995165 | Common:2; Rare:74 | ||||
chr1:91021963-91022178 | Rare:66 | ||||
chr1:91500748-91500895 | Common:2; Rare:48 | ||||
chr1:92029910-92030052 | Rare:38 | ||||
chr1:92298958-92299076 | Common:1; Rare:61; Clinvar:1 | ||||
chr1:92831958-92832113 | Common:1; Rare:82; Clinvar:6; Clinvar (benign):5 | ||||
chr1:93079089-93079291 | Common:2; Rare:87 | ||||
chr1:93180298-93180729 | Common:1; Rare:173 | ||||
chr1:93879141-93879256 | Common:1; Rare:36 |