Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29790465-29790762 | Common:2; Rare:100; Clinvar (benign):1 | ||||
chr16:29805494-29805700 | Common:2; Rare:92 | ||||
chr16:29807828-29808165 | Common:2; Rare:186 | ||||
chr16:29899170-29899495 | Common:2; Rare:50 | ||||
chr16:29900081-29900658 | Common:5; Rare:142 | ||||
chr16:29961948-29962152 | Common:1; Rare:64 | ||||
chr16:29995589-29995707 | Common:1; Rare:55 | ||||
chr16:29996070-29996283 | Common:2; Rare:76 | ||||
chr16:30064249-30064479 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr16:30065579-30065861 | Rare:92 | ||||
chr16:30075894-30076040 | Rare:50 | ||||
chr16:30123099-30123375 | Common:6; Rare:78 | ||||
chr16:30193654-30193913 | |||||
chr16:30355207-30355434 | Common:1; Rare:79 | ||||
chr16:30407475-30407636 | Rare:55 |