Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:216081783-216081877 | Rare:25 | ||||
chr2:216412245-216412561 | Common:3; Rare:74; Clinvar (benign):2 | ||||
chr2:216412664-216412786 | Rare:14 | ||||
chr2:216498754-216499051 | Common:10; Rare:115 | ||||
chr2:218270091-218270568 | Common:5; Rare:151; Clinvar:4; Clinvar (benign):2 | ||||
chr2:218287265-218287406 | Rare:24 | ||||
chr2:218568270-218568694 | Common:5; Rare:108 | ||||
chr2:218568774-218568972 | Common:1; Rare:60 | ||||
chr2:218659334-218659767 | Common:4; Rare:107 | ||||
chr2:218671974-218672339 | Common:2; Rare:90 | ||||
chr2:219176922-219177073 | Common:4; Rare:46 | ||||
chr2:219206665-219206923 | Rare:93 | ||||
chr2:219229577-219229905 | Common:2; Rare:101 | ||||
chr2:219245407-219245516 | Rare:28 | ||||
chr2:219498663-219498938 | Common:2; Rare:62 |