Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1309381-1309712 | Rare:116 | ||||
chr16:1533487-1533688 | Common:1; Rare:40 | ||||
chr16:1706056-1706281 | Common:1; Rare:64 | ||||
chr16:1943189-1943506 | Common:1; Rare:95 | ||||
chr16:1964824-1965059 | Common:6; Rare:100 | ||||
chr16:1971885-1972084 | Common:3; Rare:56 | ||||
chr16:2009678-2009891 | Common:15; Rare:91 | ||||
chr16:2047795-2048043 | Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268060-2268174 | Common:1; Rare:59 | ||||
chr16:2682362-2682645 | Rare:128 | ||||
chr16:2777240-2777371 | Common:1; Rare:49 | ||||
chr16:3112515-3112605 | Rare:21 | ||||
chr16:3134861-3135136 | Common:3; Rare:71 | ||||
chr16:3263660-3263813 | Common:1; Rare:41 | ||||
chr16:3305388-3305494 | Common:1; Rare:38 |