Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44787088-44787329 | Rare:34 | ||||
chr1:44799745-44800024 | Common:3; Rare:50 | ||||
chr1:44800059-44800507 | Common:2; Rare:116 | ||||
chr1:44800554-44800675 | Rare:27 | ||||
chr1:44800860-44801079 | Common:1; Rare:67 | ||||
chr1:44801513-44801955 | Common:2; Rare:138 | ||||
chr1:44806920-44807660 | Common:2; Rare:133 | ||||
chr1:44807756-44808009 | Common:1; Rare:61 | ||||
chr1:44810195-44810549 | Rare:79 | ||||
chr1:44813824-44813956 | Rare:31 | ||||
chr1:44986465-44986846 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45010907-45011009 | Common:2; Rare:37 | ||||
chr1:45011170-45011452 | Common:1; Rare:69 | ||||
chr1:45012031-45012313 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45012656-45012850 | Common:1; Rare:38 |