Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16644646-16644799 | Common:1; Rare:3 | ||||
chr1:17551913-17552289 | Common:2; Rare:67 | ||||
chr1:19215465-19215676 | Common:1; Rare:37 | ||||
chr1:19622124-19622368 | Rare:46 | ||||
chr1:20651729-20651788 | Common:1; Rare:14 | ||||
chr1:20891491-20891768 | Common:2; Rare:39 | ||||
chr1:22025037-22025100 | Rare:11 | ||||
chr1:22061808-22061856 | Rare:8 | ||||
chr1:23079286-23079633 | Common:4; Rare:55 | ||||
chr1:23167869-23168010 | Rare:42 | ||||
chr1:23369956-23369976 | |||||
chr1:23562428-23562692 | Common:1; Rare:79 | ||||
chr1:23695783-23696164 | Common:1; Rare:81; Clinvar (benign):1 | ||||
chr1:23745339-23745485 | Rare:30 | ||||
chr1:23795478-23795609 | Rare:30 |