Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659258-99659536 | Common:1; Rare:68 | ||||
chr10:99732070-99732329 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185878-100186198 | Rare:117 | ||||
chr10:100229551-100229652 | Rare:32 | ||||
chr10:100267601-100267746 | Common:3; Rare:46 | ||||
chr10:100286661-100286769 | Common:1; Rare:49 | ||||
chr10:100346911-100347402 | Common:1; Rare:108 | ||||
chr10:100529803-100529968 | Rare:53 | ||||
chr10:100912772-100913009 | Common:1; Rare:67 | ||||
chr10:100969191-100969570 | Common:4; Rare:97 | ||||
chr10:100987440-100987590 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100997020-100997132 | Rare:33 | ||||
chr10:101031139-101031292 | Rare:33 | ||||
chr10:101588211-101588338 | Rare:51 | ||||
chr10:101694831-101694893 | Common:1; Rare:9; Clinvar (benign):1 |