Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:11165356-11165495 | Rare:44 | ||||
chr10:12042760-12042865 | Rare:32 | ||||
chr10:12043171-12043403 | Common:2; Rare:66 | ||||
chr10:12068680-12069018 | Common:2; Rare:119 | ||||
chr10:12129456-12129726 | Rare:109 | ||||
chr10:12195797-12195967 | Rare:42 | ||||
chr10:12349739-12349821 | Common:1; Rare:35 | ||||
chr10:13099717-13099796 | Rare:20 | ||||
chr10:13099941-13100251 | Common:3; Rare:76; Clinvar:3; Clinvar (benign):5 | ||||
chr10:13348013-13348284 | Rare:85 | ||||
chr10:13707552-13707792 | Common:1; Rare:53 | ||||
chr10:14008150-14008336 | Rare:48 | ||||
chr10:14604283-14604603 | Common:6; Rare:141 | ||||
chr10:14838016-14838393 | Common:2; Rare:107 | ||||
chr10:14878604-14878886 | Common:2; Rare:91 |