Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:176111818-176111941 | Common:2; Rare:22 | ||||
chr2:176117240-176117582 | Rare:136; Clinvar:4; Clinvar (benign):1 | ||||
chr2:176118572-176118943 | Common:5; Rare:81 | ||||
chr2:176132750-176132899 | Common:2; Rare:22 | ||||
chr2:176135907-176136047 | Common:1; Rare:25 | ||||
chr2:176148938-176149146 | Rare:27 | ||||
chr2:176150295-176150528 | Common:1; Rare:57 | ||||
chr2:176637574-176637762 | Common:3; Rare:68 | ||||
chr2:177973788-177973982 | |||||
chr2:178555119-178555219 | Rare:27; Clinvar:1; Clinvar (benign):2 | ||||
chr2:178592192-178592451 | Common:1; Rare:67; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:178605176-178605441 | Common:1; Rare:55; Clinvar:7; Clinvar (pathogenic):1 | ||||
chr2:178611233-178611459 | Rare:65; Clinvar:9; Clinvar (benign):2 | ||||
chr2:178616994-178617136 | Rare:49; Clinvar:7; Clinvar (benign):2 | ||||
chr2:178629597-178629728 | Rare:30 |