Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21176636-21177117 | Rare:138 | ||||
chr1:21278755-21279170 | Common:1; Rare:94 | ||||
chr1:21279176-21279742 | Rare:156 | ||||
chr1:21279913-21280176 | Common:1; Rare:44 | ||||
chr1:21290076-21290267 | Rare:60 | ||||
chr1:21290273-21290556 | Common:2; Rare:64 | ||||
chr1:21345381-21345673 | Common:3; Rare:100 | ||||
chr1:21345874-21346015 | Common:16; Rare:65 | ||||
chr1:21781893-21782095 | Common:1; Rare:46 | ||||
chr1:21782810-21783288 | Common:3; Rare:148 | ||||
chr1:21783535-21783784 | Common:3; Rare:83 | ||||
chr1:21830125-21830334 | Common:1; Rare:46 | ||||
chr1:21830512-21830802 | Common:2; Rare:43 | ||||
chr1:21830853-21830900 | Rare:8 | ||||
chr1:21830902-21831110 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):3 |