Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16018018-16018242 | Common:5; Rare:76 | ||||
chr1:16352420-16352752 | Common:4; Rare:138 | ||||
chr1:17618263-17618424 | Common:2; Rare:37 | ||||
chr1:18902529-18902796 | Rare:85; Clinvar:7 | ||||
chr1:19210156-19210410 | Rare:96 | ||||
chr1:19251510-19251857 | Common:6; Rare:115 | ||||
chr1:19312135-19312333 | Common:5; Rare:86 | ||||
chr1:19485442-19485743 | Common:1; Rare:104 | ||||
chr1:20661406-20661705 | Common:1; Rare:107; Clinvar:3; Clinvar (benign):4 | ||||
chr1:20786636-20786861 | Rare:88 | ||||
chr1:20787226-20787416 | Rare:95 | ||||
chr1:21345476-21345674 | Common:1; Rare:75 | ||||
chr1:23424563-23424897 | Common:1; Rare:92 | ||||
chr1:23559427-23559643 | Common:1; Rare:93 | ||||
chr1:23691718-23691826 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 |