Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35008625-35008774 | Rare:33 | ||||
chr14:35103717-35103960 | Rare:29 | ||||
chr14:35401360-35401556 | Rare:40 | ||||
chr14:49585036-49585065 | Rare:10 | ||||
chr14:49618394-49618724 | Common:4; Rare:68 | ||||
chr14:49622368-49622589 | Rare:50; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:49622603-49622872 | Rare:63; Clinvar (benign):1 | ||||
chr14:49633938-49634090 | Common:1; Rare:66; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49634306-49634477 | Common:1; Rare:83; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862862-49863042 | Rare:64 | ||||
chr14:50000173-50000287 | Common:2; Rare:22 | ||||
chr14:50000874-50001111 | Rare:46 | ||||
chr14:50001277-50001392 | Common:2; Rare:28 | ||||
chr14:50453349-50453630 | Rare:48 | ||||
chr14:50479117-50479296 | Common:3; Rare:28 |