Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49622607-49622871 | Rare:60; Clinvar (benign):1 | ||||
chr14:49633956-49634043 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49634281-49634469 | Common:1; Rare:92; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:49799476-49799660 | Rare:59 | ||||
chr14:51249523-51249763 | Common:4; Rare:71 | ||||
chr14:52315012-52315346 | Rare:113 | ||||
chr14:55766588-55766785 | Rare:30 | ||||
chr14:58265808-58265992 | Rare:40 | ||||
chr14:58271587-58271867 | Rare:72 | ||||
chr14:67615597-67615628 | Common:1; Rare:9 | ||||
chr14:73245963-73246111 | Common:2; Rare:62 | ||||
chr14:77024575-77024611 | Rare:8 | ||||
chr14:77025297-77025324 | Rare:6 | ||||
chr14:77025335-77025376 | Rare:17 | ||||
chr14:77026772-77026976 | Rare:92 |