Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97445973-97446229 | Rare:69 | ||||
chr10:97498694-97498989 | Common:2; Rare:86 | ||||
chr10:97633455-97633586 | Common:1; Rare:35 | ||||
chr10:97687223-97687515 | Common:5; Rare:90 | ||||
chr10:98134536-98134688 | Common:1; Rare:54 | ||||
chr10:98446878-98447037 | Rare:45 | ||||
chr10:99430611-99430940 | Common:3; Rare:75 | ||||
chr10:99659239-99659536 | Common:1; Rare:75 | ||||
chr10:99732059-99732331 | Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185888-100186182 | Rare:108 | ||||
chr10:100229515-100229668 | Rare:57 | ||||
chr10:100267616-100267761 | Common:2; Rare:43 | ||||
chr10:100286605-100286753 | Common:5; Rare:84 | ||||
chr10:100346921-100347407 | Common:2; Rare:108 | ||||
chr10:100529803-100529972 | Rare:54 |