Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:85027620-85027801 | Common:1; Rare:94 | ||||
chr16:85799109-85799196 | Common:1; Rare:29 | ||||
chr16:85799312-85799760 | Common:3; Rare:138 | ||||
chr16:86555180-86555283 | Rare:53 | ||||
chr16:87765919-87766044 | Rare:48 | ||||
chr16:88570150-88570461 | Common:2; Rare:117 | ||||
chr16:88650986-88651138 | Common:1; Rare:50; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:88663070-88663382 | Common:9; Rare:130 | ||||
chr16:88856891-88857161 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
chr16:89217632-89217754 | Common:1; Rare:54 | ||||
chr16:89508325-89508411 | Rare:46 | ||||
chr16:89560524-89560725 | Rare:90 | ||||
chr16:89657654-89657849 | Common:1; Rare:100 | ||||
chr16:89686574-89686704 | Common:6; Rare:59 | ||||
chr16:89972478-89972605 | Common:1; Rare:41 |