Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16913883-16914115 | Common:8; Rare:47 | ||||
chr1:17588408-17588472 | Rare:21 | ||||
chr1:19076778-19077192 | Rare:96 | ||||
chr1:25875492-25875731 | Rare:66 | ||||
chr1:26863732-26864248 | Common:1; Rare:125 | ||||
chr1:36180053-36180355 | Common:2; Rare:75 | ||||
chr1:39956888-39957170 | Rare:60 | ||||
chr1:42929761-42930018 | Common:2; Rare:65; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):5 | ||||
chr1:43609122-43609426 | Common:2; Rare:79 | ||||
chr1:44644732-44645008 | Common:1; Rare:58 | ||||
chr1:51518031-51518305 | Rare:56 | ||||
chr1:58575778-58576202 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):6 | ||||
chr1:58576204-58577133 | Common:5; Rare:358; Clinvar:4; Clinvar (benign):5 | ||||
chr1:58782299-58782785 | Common:2; Rare:167; Clinvar:1 | ||||
chr1:58783054-58783125 | Rare:21 |