Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:173965256-173965508 | Common:1; Rare:87 | ||||
chr2:174395618-174395808 | Common:2; Rare:60 | ||||
chr2:176002221-176002398 | Common:2; Rare:74 | ||||
chr2:177212613-177212821 | Common:1; Rare:88 | ||||
chr2:177263402-177263595 | Rare:45 | ||||
chr2:177264533-177264813 | Common:2; Rare:81 | ||||
chr2:177392672-177392776 | Rare:22 | ||||
chr2:178194619-178194666 | Rare:10 | ||||
chr2:178450735-178450897 | Rare:54 | ||||
chr2:178451090-178451363 | Common:6; Rare:82; Clinvar:4; Clinvar (benign):3 | ||||
chr2:186485987-186486364 | Common:3; Rare:110 | ||||
chr2:186589926-186590029 | Rare:30 | ||||
chr2:186590182-186590355 | Rare:50 | ||||
chr2:189580764-189580932 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
chr2:189783973-189784078 | Common:2; Rare:35 |