Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26695552-26695848 | Common:2; Rare:227 | ||||
chr1:26695869-26696169 | Rare:203 | ||||
chr1:26696197-26696669 | Common:5; Rare:245; Clinvar:5; Clinvar (benign):5 | ||||
chr1:26787775-26788265 | Common:9; Rare:376; Clinvar:6; Clinvar (benign):6 | ||||
chr1:26826493-26826803 | Rare:257 | ||||
chr1:26826820-26827798 | Common:3; Rare:249 | ||||
chr1:26862946-26863210 | Rare:112 | ||||
chr1:26863365-26863476 | Rare:32 | ||||
chr1:26863456-26863969 | Common:5; Rare:308 | ||||
chr1:26889380-26889960 | Rare:481 | ||||
chr1:26890178-26890413 | Common:3; Rare:263 | ||||
chr1:26900001-26900255 | Rare:223 | ||||
chr1:26900377-26900614 | Rare:209 | ||||
chr1:26921507-26921879 | Common:9; Rare:314 | ||||
chr1:26945240-26945640 | Common:2; Rare:188 |