Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70169289-70169347 | Common:1; Rare:8 | ||||
chr10:70169710-70169958 | Common:1; Rare:42 | ||||
chr10:71825809-71825917 | Rare:32; Clinvar (pathogenic):1 | ||||
chr10:71965257-71965352 | Common:1; Rare:23 | ||||
chr10:72220367-72220564 | Rare:32 | ||||
chr10:72352258-72352305 | Common:2; Rare:3 | ||||
chr10:72352848-72352927 | Rare:19 | ||||
chr10:72743266-72743469 | Common:1; Rare:36 | ||||
chr10:73027649-73027902 | Common:6; Rare:36 | ||||
chr10:73139392-73139646 | Common:2; Rare:69 | ||||
chr10:73152120-73152331 | Common:1; Rare:48 | ||||
chr10:73247239-73247365 | Rare:66 | ||||
chr10:73383330-73383634 | Rare:75 | ||||
chr10:73495141-73495317 | Common:1; Rare:42 | ||||
chr10:73730430-73730610 | Common:1; Rare:44 |