Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:88759753-88760042 | Rare:49 | ||||
chr10:88812936-88813198 | Rare:70 | ||||
chr10:88817031-88817344 | Common:2; Rare:52 | ||||
chr10:88939603-88939822 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr10:91347711-91347771 | Rare:11 | ||||
chr10:91807525-91807691 | Rare:30 | ||||
chr10:91952615-91952630 | Rare:2 | ||||
chr10:92240658-92240929 | Common:1; Rare:67 | ||||
chr10:93333876-93333942 | Rare:21 | ||||
chr10:97400028-97400229 | Common:3; Rare:36 | ||||
chr10:97432172-97432465 | Common:1; Rare:69 | ||||
chr10:97679181-97679248 | Rare:10 | ||||
chr10:97680004-97680247 | Common:1; Rare:30 | ||||
chr10:100970120-100970319 | Rare:45 | ||||
chr10:101031924-101032089 | Rare:43 |