Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1516588-1516994 | Common:2; Rare:141 | ||||
chr17:1628812-1629005 | Rare:68 | ||||
chr17:1829822-1830027 | Common:4; Rare:86 | ||||
chr17:2303504-2303617 | Rare:42 | ||||
chr17:2303727-2303980 | Common:2; Rare:96 | ||||
chr17:2336413-2336550 | Rare:58 | ||||
chr17:2511812-2511925 | Common:2; Rare:31 | ||||
chr17:2593512-2593683 | Common:3; Rare:52; Clinvar (benign):2 | ||||
chr17:2593863-2593970 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
chr17:2711726-2712031 | Common:2; Rare:86 | ||||
chr17:3636235-3636743 | Common:7; Rare:140; Clinvar:5; Clinvar (benign):3 | ||||
chr17:3668546-3668820 | Common:2; Rare:107 | ||||
chr17:4142989-4143237 | Rare:87 | ||||
chr17:4143608-4143727 | Common:4; Rare:66 | ||||
chr17:4263943-4264015 | Rare:33 |