Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71824703-71824913 | Common:1; Rare:39 | ||||
chr10:71824947-71825044 | Rare:14 | ||||
chr10:71825051-71825303 | Common:1; Rare:61 | ||||
chr10:71825806-71825919 | Rare:34; Clinvar (pathogenic):1 | ||||
chr10:71888732-71888795 | Rare:7 | ||||
chr10:71901666-71901697 | Common:1; Rare:5 | ||||
chr10:71965256-71965355 | Common:1; Rare:25 | ||||
chr10:72190310-72190525 | Rare:33 | ||||
chr10:72272829-72273085 | Common:1; Rare:58 | ||||
chr10:72298062-72298290 | Common:1; Rare:58 | ||||
chr10:72352847-72353227 | Common:3; Rare:62 | ||||
chr10:72353831-72353850 | Rare:4 | ||||
chr10:72450834-72451011 | Common:4; Rare:28 | ||||
chr10:72511989-72512095 | Rare:23 | ||||
chr10:72515839-72516056 | Rare:27 |