Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23415382-23415834 | Common:1; Rare:140; Clinvar:23; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
chr14:23425795-23426064 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):7 | ||||
chr14:23431420-23431590 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr14:24259365-24259543 | Rare:38 | ||||
chr14:31102976-31103332 | Common:2; Rare:69 | ||||
chr14:32203245-32203667 | Common:13; Rare:186 | ||||
chr14:34874125-34874227 | Common:1; Rare:28 | ||||
chr14:36136150-36136609 | Common:1; Rare:66 | ||||
chr14:36454609-36454684 | Common:1; Rare:9 | ||||
chr14:36505958-36506092 | Rare:30 | ||||
chr14:36508295-36508457 | Rare:30 | ||||
chr14:36510439-36510745 | Rare:47 | ||||
chr14:36514853-36514961 | Rare:18 | ||||
chr14:36516265-36516407 | Common:1; Rare:26 | ||||
chr14:36522502-36522648 | Common:1; Rare:28 |