Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:18801442-18801856 | Common:4; Rare:143 | ||||
chr16:18925961-18925969 | |||||
chr16:19067586-19067685 | Common:2; Rare:56; Clinvar:1 | ||||
chr16:19067808-19067929 | Common:2; Rare:31 | ||||
chr16:19183354-19183535 | Rare:32 | ||||
chr16:19521609-19521731 | Rare:33 | ||||
chr16:19555326-19555729 | Common:1; Rare:162 | ||||
chr16:20763939-20764063 | Common:2; Rare:21 | ||||
chr16:20806331-20806546 | Rare:76 | ||||
chr16:20899596-20899924 | Rare:60 | ||||
chr16:20900222-20900850 | Common:4; Rare:148 | ||||
chr16:21233567-21233739 | Rare:36 | ||||
chr16:21652597-21652723 | Rare:33 | ||||
chr16:21953028-21953455 | Common:1; Rare:110; Clinvar (benign):3 | ||||
chr16:22206542-22206560 | Rare:4 |