Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:71866973-71867102 | Rare:23 | ||||
chr13:72727599-72727953 | Common:4; Rare:131 | ||||
chr13:72781932-72782191 | Rare:90 | ||||
chr13:76992041-76992194 | Common:1; Rare:73; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
chr13:77027137-77027289 | Common:5; Rare:47 | ||||
chr13:95301431-95301529 | Rare:26 | ||||
chr13:95676887-95677145 | Common:2; Rare:97 | ||||
chr13:97222154-97222338 | Rare:35 | ||||
chr13:97976387-97976685 | Common:1; Rare:105 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:99307397-99307425 | Rare:3 | ||||
chr13:100088936-100089134 | Rare:75; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674759-100675040 | Common:3; Rare:112 | ||||
chr13:100675077-100675191 | Common:1; Rare:46 | ||||
chr13:102596773-102597035 | Common:1; Rare:122 |