Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:17753829-17754125 | Common:2; Rare:85 | ||||
chr2:26244602-26244965 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):7 | ||||
chr2:27212252-27212364 | Common:1; Rare:57 | ||||
chr2:27323058-27323154 | Rare:23 | ||||
chr2:27370303-27370636 | Common:1; Rare:135 | ||||
chr2:27582797-27583045 | Rare:77 | ||||
chr2:27628833-27629058 | Common:1; Rare:85 | ||||
chr2:27663607-27663904 | Rare:105 | ||||
chr2:28870275-28870454 | Rare:64 | ||||
chr2:32039761-32039833 | Rare:25 | ||||
chr2:37084328-37084524 | Common:3; Rare:69 | ||||
chr2:37231570-37231674 | Common:3; Rare:50; Clinvar (benign):3 | ||||
chr2:46617025-46617238 | Common:6; Rare:80 | ||||
chr2:53786862-53787078 | Rare:71 | ||||
chr2:55050495-55050784 | Common:3; Rare:88 |