Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:52617322-52617535 | Rare:51 | ||||
chr13:73059297-73059586 | Rare:71 | ||||
chr13:94713439-94713642 | Rare:40 | ||||
chr14:24258321-24258647 | Rare:86; Clinvar:3; Clinvar (pathogenic):5 | ||||
chr14:24259109-24259375 | Rare:65; Clinvar:2; Clinvar (pathogenic):3 | ||||
chr14:31250150-31250323 | Common:1; Rare:25 | ||||
chr14:49633956-49634070 | Common:1; Rare:45; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862642-49863028 | Common:1; Rare:178 | ||||
chr14:68565221-68565361 | Rare:11 | ||||
chr14:73245985-73246092 | Common:2; Rare:43 | ||||
chr14:75259171-75259383 | Rare:42 | ||||
chr14:75469176-75469417 | Common:1; Rare:65 | ||||
chr14:75654948-75655020 | Rare:23 | ||||
chr14:89203603-89203661 | Common:2; Rare:13 | ||||
chr14:100130857-100130914 | Common:2; Rare:9 |