Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:95907793-95907955 | Common:3; Rare:54 | ||||
chr10:96129988-96130068 | Common:1; Rare:24 | ||||
chr10:96832095-96832299 | Rare:78 | ||||
chr10:97334683-97334876 | Common:2; Rare:78 | ||||
chr10:97426051-97426307 | Common:2; Rare:115 | ||||
chr10:97445975-97446223 | Rare:66 | ||||
chr10:97498387-97498555 | Common:2; Rare:64 | ||||
chr10:97498644-97499057 | Common:2; Rare:121 | ||||
chr10:97687175-97687490 | Common:6; Rare:94 | ||||
chr10:97713326-97713478 | Rare:34 | ||||
chr10:98268175-98268433 | Common:2; Rare:64 | ||||
chr10:98425662-98425952 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:98446878-98446971 | Rare:23 | ||||
chr10:99430622-99430996 | Common:3; Rare:89 | ||||
chr10:99532746-99533058 | Common:5; Rare:70 |