Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3065207-3065424 | Common:3; Rare:59 | ||||
chr16:3112454-3112595 | Rare:33 | ||||
chr16:3134841-3135125 | Common:2; Rare:71 | ||||
chr16:3305403-3305514 | Common:1; Rare:37 | ||||
chr16:3443461-3443732 | Common:3; Rare:93 | ||||
chr16:3457914-3458126 | Common:2; Rare:102 | ||||
chr16:4425749-4425879 | Common:1; Rare:61 | ||||
chr16:4476273-4476452 | Common:3; Rare:66 | ||||
chr16:4693476-4693729 | Common:2; Rare:110 | ||||
chr16:4734237-4734534 | Rare:92 | ||||
chr16:8797631-8797877 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr16:10743742-10743861 | Rare:45 | ||||
chr16:11587160-11587428 | Common:1; Rare:71 | ||||
chr16:11851513-11851645 | Rare:64 | ||||
chr16:14630197-14630428 | Rare:102 |