Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:18801456-18801830 | Common:4; Rare:132 | ||||
chr16:19555579-19555726 | Common:1; Rare:79 | ||||
chr16:20806432-20806627 | Rare:65 | ||||
chr16:21953000-21953419 | Common:1; Rare:106; Clinvar (benign):3 | ||||
chr16:23641223-23641517 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24729611-24729739 | Common:6; Rare:69 | ||||
chr16:25015329-25015461 | Common:2; Rare:46 | ||||
chr16:25111462-25111762 | Common:2; Rare:70 | ||||
chr16:27268713-27268872 | Common:1; Rare:57 | ||||
chr16:27549889-27550167 | Common:2; Rare:103 | ||||
chr16:28822629-28822739 | Rare:38 | ||||
chr16:28846256-28846643 | Common:2; Rare:131; Clinvar:6; Clinvar (benign):6 | ||||
chr16:28925167-28925408 | Rare:79 | ||||
chr16:28974610-28974792 | Common:1; Rare:68 | ||||
chr16:29995606-29995707 | Rare:45 |