Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:15727091-15727215 | Common:1; Rare:34 | ||||
chr16:15728493-15728544 | Rare:15 | ||||
chr16:15735131-15735787 | Common:4; Rare:173; Clinvar:11; Clinvar (benign):6 | ||||
chr16:15735984-15736004 | Rare:3 | ||||
chr16:15747820-15747974 | Common:2; Rare:43; Clinvar:3; Clinvar (benign):3 | ||||
chr16:15759534-15759797 | Common:1; Rare:74; Clinvar:5; Clinvar (benign):6 | ||||
chr16:18347953-18348023 | Common:1; Rare:22 | ||||
chr16:19120559-19120838 | Common:5; Rare:65 | ||||
chr16:21501897-21501920 | Rare:2 | ||||
chr16:21820390-21820560 | Rare:50 | ||||
chr16:27330653-27330848 | Common:2; Rare:37 | ||||
chr16:29595047-29595147 | Common:6; Rare:58 | ||||
chr16:29812954-29813026 | Rare:15; Clinvar (benign):1 | ||||
chr16:29819517-29819596 | Common:1; Rare:29 | ||||
chr16:30335346-30335481 | Common:1; Rare:48 |