Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:18140449-18140801 | Common:4; Rare:110; Clinvar:3; Clinvar (benign):5 | ||||
chr10:18651573-18651675 | Common:1; Rare:36 | ||||
chr10:18659237-18659571 | Common:2; Rare:110 | ||||
chr10:19815785-19815926 | Rare:38 | ||||
chr10:19816248-19816654 | Common:6; Rare:88 | ||||
chr10:21525617-21525905 | Rare:69 | ||||
chr10:21526398-21526576 | Common:1; Rare:57 | ||||
chr10:21533964-21534341 | Common:3; Rare:155 | ||||
chr10:22316228-22316518 | Common:2; Rare:134 | ||||
chr10:22321358-22321615 | Rare:89 | ||||
chr10:22325513-22325856 | Rare:137 | ||||
chr10:24208772-24209258 | Common:2; Rare:138 | ||||
chr10:24722704-24722846 | Common:1; Rare:37 | ||||
chr10:27100396-27100591 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154310-27154480 | Rare:45 |