Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150150119-150150286 | Common:2; Rare:58 | ||||
chr1:150234654-150234750 | Rare:18 | ||||
chr1:150267435-150267741 | Rare:55 | ||||
chr1:150267746-150268084 | Common:2; Rare:77 | ||||
chr1:150268279-150268434 | Rare:27 | ||||
chr1:150487209-150487473 | Common:5; Rare:72; Clinvar (benign):3 | ||||
chr1:150578487-150578644 | Common:1; Rare:51 | ||||
chr1:150578835-150579127 | Common:3; Rare:114 | ||||
chr1:150579581-150579918 | Common:11; Rare:101 | ||||
chr1:150629055-150629405 | Common:1; Rare:113 | ||||
chr1:150629541-150629822 | Rare:55 | ||||
chr1:150765707-150765916 | Common:2; Rare:20 | ||||
chr1:150926148-150926427 | Rare:87 | ||||
chr1:150974650-150974946 | Common:2; Rare:95 | ||||
chr1:151008181-151008586 | Common:2; Rare:105 |