Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:21456056-21456307 | Common:3; Rare:66 | ||||
chr14:21476878-21477267 | Common:2; Rare:124 | ||||
chr14:21511277-21511534 | Rare:67 | ||||
chr14:21526223-21526466 | Rare:50 | ||||
chr14:22598203-22598316 | Rare:39 | ||||
chr14:22766508-22766757 | Common:1; Rare:140 | ||||
chr14:22872092-22872222 | Common:2; Rare:29 | ||||
chr14:22929357-22929620 | Rare:60 | ||||
chr14:22982498-22982941 | Common:4; Rare:155 | ||||
chr14:23095084-23095594 | Common:3; Rare:228 | ||||
chr14:23154298-23154489 | Common:2; Rare:44 | ||||
chr14:23286087-23286396 | Common:1; Rare:66 | ||||
chr14:23306712-23306885 | Common:1; Rare:39 | ||||
chr14:23407539-23407817 | Rare:45; Clinvar (benign):3 | ||||
chr14:23408187-23408655 | Common:3; Rare:102; Clinvar (benign):3 |