Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3611558-3611815 | Common:1; Rare:109; Clinvar:1 | ||||
chr16:4371588-4371882 | Common:1; Rare:97 | ||||
chr16:4425752-4425917 | Common:1; Rare:89 | ||||
chr16:4476304-4476481 | Common:1; Rare:67 | ||||
chr16:4507516-4507847 | Common:1; Rare:89 | ||||
chr16:4538397-4538649 | Common:2; Rare:89 | ||||
chr16:4538726-4538919 | Rare:73 | ||||
chr16:4614853-4615073 | Common:1; Rare:63 | ||||
chr16:4693476-4693735 | Common:2; Rare:114 | ||||
chr16:4734134-4734538 | Common:1; Rare:132 | ||||
chr16:4767126-4767360 | Common:1; Rare:78 | ||||
chr16:4958063-4958340 | Common:6; Rare:76 | ||||
chr16:5033926-5033976 | Rare:17 | ||||
chr16:5071791-5071856 | Rare:33; Clinvar (benign):1 | ||||
chr16:5097737-5098032 | Common:4; Rare:100 |