Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54865595-54865860 | Common:1; Rare:46 | ||||
chr1:54883320-54883730 | Rare:118; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr1:56414530-56415090 | Common:4; Rare:112 | ||||
chr1:56461230-56461520 | Common:3; Rare:60 | ||||
chr1:56477273-56477568 | Common:3; Rare:62 | ||||
chr1:56508450-56508888 | Common:5; Rare:148 | ||||
chr1:56569410-56569920 | Common:1; Rare:90 | ||||
chr1:58816310-58816690 | Common:4; Rare:171 | ||||
chr1:58903520-58903980 | Common:2; Rare:241 | ||||
chr1:59730920-59731200 | Common:1; Rare:55 | ||||
chr1:62424510-62424790 | Common:2; Rare:54 | ||||
chr1:62691140-62691550 | Rare:133 | ||||
chr1:62754405-62755190 | Common:8; Rare:160 | ||||
chr1:65066700-65067050 | Rare:108 | ||||
chr1:75677310-75677940 | Common:14; Rare:205 |