Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596742-19597052 | Common:3; Rare:107 | ||||
chr1:19799878-19799989 | Common:1; Rare:45 | ||||
chr1:20661346-20661727 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21290421-21290495 | Common:1; Rare:18 | ||||
chr1:21345483-21345674 | Rare:71 | ||||
chr1:23344226-23344576 | Common:2; Rare:116 | ||||
chr1:23368216-23368513 | Common:1; Rare:85 | ||||
chr1:23559479-23559643 | Common:1; Rare:68 | ||||
chr1:23778250-23778537 | Common:9; Rare:138 | ||||
chr1:23791041-23791217 | Rare:54 | ||||
chr1:23800753-23800908 | Common:1; Rare:48 | ||||
chr1:23825411-23825504 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23868273-23868531 | Common:5; Rare:70; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23959080-23959204 | Common:2; Rare:23 | ||||
chr1:23959641-23959868 | Common:2; Rare:63 |