Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674075-44674343 | Common:1; Rare:79 | ||||
chr1:44674362-44674777 | Common:3; Rare:121 | ||||
chr1:44739536-44740019 | Common:3; Rare:177 | ||||
chr1:44740085-44740181 | Rare:25 | ||||
chr1:44774993-44775085 | Rare:18 | ||||
chr1:44775416-44775714 | Common:3; Rare:115 | ||||
chr1:44775850-44775893 | Rare:20 | ||||
chr1:44776014-44776503 | Common:1; Rare:123 | ||||
chr1:44799722-44799992 | Common:3; Rare:52 | ||||
chr1:44800100-44800496 | Common:2; Rare:101 | ||||
chr1:44808509-44808538 | Rare:8 | ||||
chr1:44808639-44808688 | Rare:10 | ||||
chr1:44843143-44843293 | Rare:41 | ||||
chr1:44986510-44986876 | Common:2; Rare:74; Clinvar (benign):1 | ||||
chr1:45011294-45011458 | Common:1; Rare:40 |