Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1706044-1706258 | Common:2; Rare:65 | ||||
chr16:1771488-1771602 | Rare:52 | ||||
chr16:1773064-1773213 | Rare:50; Clinvar (pathogenic):1 | ||||
chr16:1782508-1783015 | Common:4; Rare:168 | ||||
chr16:1827157-1827255 | Common:1; Rare:50 | ||||
chr16:1943117-1943489 | Common:1; Rare:118 | ||||
chr16:1964806-1965003 | Common:6; Rare:90 | ||||
chr16:1971879-1972106 | Common:3; Rare:66 | ||||
chr16:2026716-2026919 | Common:1; Rare:76 | ||||
chr16:2047721-2048056 | Rare:169; Clinvar:2; Clinvar (benign):4 | ||||
chr16:2268056-2268210 | Common:1; Rare:71 | ||||
chr16:2429121-2429478 | Common:2; Rare:117 | ||||
chr16:2459994-2460126 | Rare:33 | ||||
chr16:2474983-2475157 | Rare:57; Clinvar (benign):2 | ||||
chr16:2682367-2682557 | Rare:78 |