Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:93227139-93227347 | Rare:44; Clinvar:3 | ||||
chr13:94601600-94601907 | Common:3; Rare:87 | ||||
chr13:95676828-95677172 | Common:2; Rare:132 | ||||
chr13:96053327-96053515 | Common:2; Rare:87 | ||||
chr13:97222185-97222369 | Rare:31 | ||||
chr13:97434614-97434717 | Rare:16 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088859-100089117 | Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674778-100675045 | Common:3; Rare:108 | ||||
chr13:101416336-101416660 | Rare:63 | ||||
chr13:102402351-102402498 | Rare:31 | ||||
chr13:102596785-102597035 | Common:1; Rare:119 | ||||
chr13:102773736-102773842 | Rare:52 | ||||
chr13:102798998-102799183 | Rare:40 | ||||
chr13:102845719-102846089 | Common:9; Rare:99; Clinvar:2; Clinvar (benign):4 |