Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77457529-77457791 | Common:1; Rare:87 | ||||
chr14:77616769-77617084 | Common:1; Rare:69 | ||||
chr14:77707985-77708117 | Rare:63 | ||||
chr14:77761131-77761237 | Rare:46 | ||||
chr14:81220871-81221069 | Common:1; Rare:94 | ||||
chr14:81533788-81534104 | Rare:79 | ||||
chr14:87993079-87993301 | Common:4; Rare:102; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr14:88005090-88005150 | Rare:8 | ||||
chr14:89954711-89954937 | Rare:58 | ||||
chr14:90331906-90332203 | Common:1; Rare:86 | ||||
chr14:90396895-90397052 | Common:1; Rare:85 | ||||
chr14:91114361-91114699 | Common:1; Rare:49 | ||||
chr14:91510285-91510652 | Common:1; Rare:116 | ||||
chr14:92040026-92040192 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr14:92121656-92122276 | Common:5; Rare:194 |