Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:3782457-3782697 | Rare:51 | ||||
chr10:3785143-3785551 | Common:4; Rare:152 | ||||
chr10:7787958-7788245 | Common:1; Rare:119 | ||||
chr10:8053474-8053657 | Rare:55 | ||||
chr10:12195797-12196241 | Rare:120 | ||||
chr10:13099987-13100248 | Common:3; Rare:65; Clinvar:3; Clinvar (benign):5 | ||||
chr10:13707172-13707423 | Common:3; Rare:49 | ||||
chr10:14008157-14008367 | Rare:51 | ||||
chr10:14604241-14604544 | Common:4; Rare:134 | ||||
chr10:14838058-14838355 | Common:2; Rare:77 | ||||
chr10:14878637-14878891 | Common:2; Rare:76 | ||||
chr10:14954023-14954194 | Rare:61 | ||||
chr10:15097303-15097378 | Common:1; Rare:34 | ||||
chr10:15860455-15860589 | Rare:37 | ||||
chr10:16817319-16817744 | Common:5; Rare:151 |