Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97426044-97426299 | Common:2; Rare:111 | ||||
chr10:97445975-97446226 | Rare:66 | ||||
chr10:97498344-97498557 | Common:2; Rare:93 | ||||
chr10:97498694-97499040 | Common:2; Rare:99 | ||||
chr10:97737023-97737227 | Common:1; Rare:70 | ||||
chr10:98134833-98134940 | Common:1; Rare:32 | ||||
chr10:98268183-98268442 | Common:3; Rare:67 | ||||
chr10:99430556-99430936 | Common:4; Rare:92 | ||||
chr10:99659203-99659583 | Common:2; Rare:99 | ||||
chr10:99732070-99732340 | Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
chr10:99782468-99782845 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100081405-100081578 | Rare:74 | ||||
chr10:100185718-100186198 | Rare:161 | ||||
chr10:100229528-100229673 | Rare:56 | ||||
chr10:100267616-100267733 | Common:2; Rare:38 |