Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:11004853-11005427 | Common:4; Rare:132 | ||||
chr10:11164741-11165065 | Rare:70 | ||||
chr10:12068753-12069018 | Common:2; Rare:101 | ||||
chr10:12129444-12129726 | Rare:114 | ||||
chr10:12195838-12196251 | Rare:112 | ||||
chr10:13099711-13099925 | Rare:51 | ||||
chr10:13099945-13100247 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):5 | ||||
chr10:13300038-13300153 | Rare:46; Clinvar:1 | ||||
chr10:14330807-14330995 | Rare:36 | ||||
chr10:14837952-14838389 | Common:2; Rare:135 | ||||
chr10:14878647-14878891 | Common:2; Rare:71 | ||||
chr10:14954023-14954195 | Rare:61 | ||||
chr10:15097319-15097378 | Common:1; Rare:25 | ||||
chr10:15860453-15860589 | Rare:37 | ||||
chr10:16817361-16817744 | Common:4; Rare:138 |