Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:95656647-95656945 | Rare:81; Clinvar:5 | ||||
chr10:95693888-95694083 | Common:2; Rare:71; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:95907733-95907955 | Common:3; Rare:63 | ||||
chr10:96129648-96129750 | Common:1; Rare:27 | ||||
chr10:96129962-96130067 | Common:1; Rare:36 | ||||
chr10:96130219-96130362 | Rare:51 | ||||
chr10:96130418-96130657 | Common:1; Rare:71 | ||||
chr10:96832095-96832300 | Rare:79 | ||||
chr10:97334716-97334883 | Common:1; Rare:55 | ||||
chr10:97426035-97426308 | Common:2; Rare:125 | ||||
chr10:97445975-97446247 | Rare:72 | ||||
chr10:97498376-97498503 | Common:1; Rare:64 | ||||
chr10:97498694-97499048 | Common:2; Rare:102 | ||||
chr10:97633443-97633671 | Common:2; Rare:63 | ||||
chr10:97687223-97687522 | Common:5; Rare:93 |