Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100969343-100969530 | Common:3; Rare:37 | ||||
chr10:100987090-100987295 | Rare:72 | ||||
chr10:100987364-100987604 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996967-100997132 | Common:1; Rare:47 | ||||
chr10:101588144-101588333 | Rare:76 | ||||
chr10:101783287-101783506 | Rare:95 | ||||
chr10:101818393-101818762 | Common:1; Rare:99 | ||||
chr10:101839849-101839924 | Rare:25 | ||||
chr10:102056102-102056387 | Common:2; Rare:69 | ||||
chr10:102114962-102115265 | Common:2; Rare:82 | ||||
chr10:102152070-102152444 | Common:3; Rare:122 | ||||
chr10:102160259-102160586 | Common:2; Rare:98 | ||||
chr10:102395589-102395720 | Rare:36 | ||||
chr10:102420794-102420860 | Rare:15 | ||||
chr10:102714206-102714643 | Common:2; Rare:145 |