Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24215958-24216138 | Common:1; Rare:57 | ||||
chr14:24232314-24232698 | Common:8; Rare:89 | ||||
chr14:24232823-24232970 | Common:1; Rare:35 | ||||
chr14:24242556-24242767 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271457-24271609 | Common:1; Rare:45 | ||||
chr14:24299743-24299850 | Common:2; Rare:31 | ||||
chr14:24429664-24430095 | Common:3; Rare:101 | ||||
chr14:24430583-24430744 | Common:1; Rare:29 | ||||
chr14:24442661-24443046 | Common:5; Rare:121 | ||||
chr14:30622190-30622352 | Rare:59 | ||||
chr14:31025348-31025670 | Common:2; Rare:75 | ||||
chr14:31207701-31207883 | Rare:60 | ||||
chr14:32076657-32077074 | Common:3; Rare:123 | ||||
chr14:34462226-34462548 | Common:1; Rare:107 | ||||
chr14:34630087-34630260 | Common:5; Rare:83 |