Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13348045-13348357 | Rare:103 | ||||
chr10:13707544-13707738 | Rare:45 | ||||
chr10:14837974-14838341 | Common:2; Rare:104 | ||||
chr10:14878657-14878888 | Common:2; Rare:66 | ||||
chr10:14954023-14954195 | Rare:61 | ||||
chr10:15097306-15097385 | Common:1; Rare:38 | ||||
chr10:15860489-15860577 | Rare:24 | ||||
chr10:16817352-16817744 | Common:4; Rare:141 | ||||
chr10:17228583-17228675 | Common:1; Rare:28 | ||||
chr10:17229070-17229328 | Common:2; Rare:49 | ||||
chr10:17643877-17644241 | Common:2; Rare:109 | ||||
chr10:18651582-18651738 | Common:1; Rare:65 | ||||
chr10:24466416-24466549 | Rare:21 | ||||
chr10:27100461-27100580 | Common:3; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
chr10:27154323-27154486 | Rare:45 |