Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102362858-102363092 | Rare:105 | ||||
chr14:103562656-103563004 | Common:5; Rare:120; Clinvar (benign):1 | ||||
chr15:35546157-35546258 | Common:1; Rare:33 | ||||
chr15:40039109-40039278 | Rare:73 | ||||
chr15:40807454-40807656 | Common:2; Rare:60 | ||||
chr15:42273417-42273551 | Rare:51 | ||||
chr15:42548736-42548862 | Common:1; Rare:70 | ||||
chr15:43330594-43330703 | Rare:39 | ||||
chr15:43746305-43746439 | Common:1; Rare:52 | ||||
chr15:49155579-49155768 | Common:1; Rare:67 | ||||
chr15:50354885-50354998 | Rare:16 | ||||
chr15:55319091-55319232 | Common:1; Rare:35 | ||||
chr15:63121783-63121869 | Rare:30 | ||||
chr15:66504844-66505117 | Common:1; Rare:88 | ||||
chr15:67521088-67521200 | Common:1; Rare:49 |