Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:57377184-57377319 | Common:1; Rare:21 | ||||
chr16:57377332-57377533 | Rare:39 | ||||
chr16:57413446-57413877 | Common:2; Rare:63 | ||||
chr16:57446891-57447036 | Common:2; Rare:29 | ||||
chr16:57447302-57447560 | Common:4; Rare:83; Clinvar:2; Clinvar (benign):4 | ||||
chr16:57447754-57447821 | Common:1; Rare:7 | ||||
chr16:57447896-57447944 | Rare:8 | ||||
chr16:57462440-57462802 | Common:2; Rare:131 | ||||
chr16:57475903-57475959 | Rare:17 | ||||
chr16:57486459-57486578 | Common:1; Rare:48 | ||||
chr16:57487204-57487405 | Common:1; Rare:40 | ||||
chr16:57535905-57536365 | Common:2; Rare:161 | ||||
chr16:57536538-57536672 | Common:3; Rare:40 | ||||
chr16:57542391-57542730 | Common:4; Rare:63 | ||||
chr16:57735475-57735825 | Common:3; Rare:83 |