Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177837060-177837129 | Common:1; Rare:16 | ||||
chr2:188996176-188996469 | Common:12; Rare:65; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:188997170-188997389 | Common:5; Rare:56; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):4 | ||||
chr2:191846447-191846632 | Common:2; Rare:74 | ||||
chr2:191846635-191846740 | Common:2; Rare:26 | ||||
chr2:202036309-202036378 | Rare:19 | ||||
chr2:202376071-202376205 | Rare:67 | ||||
chr2:205687242-205687255 | Common:1; Rare:4 | ||||
chr2:206084401-206084658 | Common:1; Rare:55 | ||||
chr2:215367861-215368196 | Common:1; Rare:90 | ||||
chr2:215433563-215433840 | Common:1; Rare:60 | ||||
chr2:216692160-216692371 | Common:3; Rare:52 | ||||
chr2:217824958-217825015 | Rare:9 | ||||
chr2:217873404-217873483 | Rare:17 | ||||
chr2:217920900-217921157 | Common:3; Rare:45 |