Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30650839-30650966 | Rare:46 | ||||
chr16:30651407-30651637 | Rare:58 | ||||
chr16:30697892-30698235 | Common:1; Rare:145 | ||||
chr16:30698449-30698723 | Common:1; Rare:102 | ||||
chr16:30698979-30699379 | Rare:112; Clinvar (benign):1 | ||||
chr16:30762080-30762331 | Common:3; Rare:89 | ||||
chr16:30787146-30787508 | Common:1; Rare:76 | ||||
chr16:30893911-30894275 | Common:5; Rare:98 | ||||
chr16:30896439-30896644 | Common:1; Rare:50 | ||||
chr16:30923232-30923592 | Common:1; Rare:87 | ||||
chr16:30949030-30949119 | Rare:16 | ||||
chr16:31033243-31033582 | Common:2; Rare:102 | ||||
chr16:31073732-31073848 | Rare:33 | ||||
chr16:31074177-31074456 | Common:2; Rare:77 | ||||
chr16:31130278-31130502 | Rare:61 |