Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:217434197-217434346 | Rare:34 | ||||
chr2:217901881-217902175 | Common:3; Rare:47 | ||||
chr2:217978639-217978763 | Rare:37 | ||||
chr2:217978770-217978934 | Common:1; Rare:47 | ||||
chr2:217979225-217979262 | Rare:2 | ||||
chr2:218217014-218217226 | Common:1; Rare:74 | ||||
chr2:218270057-218270538 | Common:5; Rare:149; Clinvar:3; Clinvar (benign):1 | ||||
chr2:218287270-218287387 | Rare:19 | ||||
chr2:218292470-218292651 | Common:1; Rare:54 | ||||
chr2:218316568-218316753 | Common:1; Rare:18 | ||||
chr2:218322982-218323351 | Common:6; Rare:123 | ||||
chr2:218399544-218399756 | Common:1; Rare:95 | ||||
chr2:218568218-218568933 | Common:7; Rare:181 | ||||
chr2:218659339-218659363 | Rare:8 | ||||
chr2:218659597-218659740 | Rare:35 |