Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:25822208-25822378 | Rare:45 | ||||
chr2:26724008-26724251 | Common:1; Rare:48 | ||||
chr2:27025297-27025463 | Common:1; Rare:33 | ||||
chr2:27207196-27207295 | Rare:29 | ||||
chr2:27209946-27209997 | Common:1; Rare:7 | ||||
chr2:27752758-27752931 | Rare:26 | ||||
chr2:32357972-32358087 | Common:1; Rare:16 | ||||
chr2:37216159-37216411 | Rare:68 | ||||
chr2:43190661-43190873 | Rare:49 | ||||
chr2:43808373-43808543 | Common:3; Rare:27 | ||||
chr2:43820084-43820136 | Rare:15 | ||||
chr2:47790761-47791069 | Common:2; Rare:82; Clinvar:18; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
chr2:47906467-47906815 | Common:2; Rare:127 | ||||
chr2:48200813-48200952 | Rare:22 | ||||
chr2:54560448-54560597 | Common:2; Rare:47 |