Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:7787950-7788222 | Common:1; Rare:113 | ||||
chr10:12129433-12129726 | Rare:123 | ||||
chr10:12195776-12196259 | Rare:130 | ||||
chr10:13099990-13100205 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):4 | ||||
chr10:13300040-13300164 | Rare:47; Clinvar:1 | ||||
chr10:13348045-13348352 | Rare:102 | ||||
chr10:14838018-14838395 | Common:2; Rare:107 | ||||
chr10:14878657-14878891 | Common:2; Rare:67 | ||||
chr10:14954030-14954240 | Rare:70 | ||||
chr10:15860455-15860572 | Rare:34 | ||||
chr10:17228881-17229307 | Common:5; Rare:88 | ||||
chr10:17643871-17644265 | Common:2; Rare:119 | ||||
chr10:18651581-18651699 | Common:1; Rare:44 | ||||
chr10:22325491-22325671 | Common:1; Rare:80 | ||||
chr10:24466457-24466553 | Rare:15 |