Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:10301211-10301394 | Common:1; Rare:28 | ||||
chr2:12277569-12277795 | Common:1; Rare:38 | ||||
chr2:20208121-20208443 | Common:2; Rare:68 | ||||
chr2:20209422-20209742 | Common:2; Rare:59 | ||||
chr2:20215293-20215539 | Common:3; Rare:40 | ||||
chr2:20447729-20447872 | Rare:40 | ||||
chr2:20448112-20448426 | Common:2; Rare:84 | ||||
chr2:20480937-20481166 | Common:1; Rare:38 | ||||
chr2:20593377-20593783 | Common:6; Rare:69 | ||||
chr2:21015040-21015552 | Common:4; Rare:133; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr2:21029620-21030024 | Common:1; Rare:99; Clinvar:3; Clinvar (benign):10 | ||||
chr2:21042855-21043084 | Rare:40 | ||||
chr2:23198918-23199230 | Common:1; Rare:64 | ||||
chr2:23208509-23208667 | Common:1; Rare:35 | ||||
chr2:24074130-24074247 | Rare:33 |