Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12195781-12195974 | Rare:47 | ||||
chr10:13099966-13100259 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13707565-13707761 | Common:1; Rare:43 | ||||
chr10:14838007-14838386 | Common:2; Rare:107 | ||||
chr10:14878637-14878897 | Common:2; Rare:78 | ||||
chr10:14954023-14954194 | Rare:61 | ||||
chr10:15097039-15097401 | Common:6; Rare:160 | ||||
chr10:15860455-15860589 | Rare:37 | ||||
chr10:16817478-16817777 | Common:1; Rare:98 | ||||
chr10:17229014-17229291 | Common:2; Rare:51 | ||||
chr10:17643866-17644214 | Common:1; Rare:104 | ||||
chr10:18651553-18651778 | Common:1; Rare:92 | ||||
chr10:21533964-21534236 | Common:1; Rare:100 | ||||
chr10:24208834-24208922 | Rare:30 | ||||
chr10:24239036-24239216 | Rare:13 |