Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:79598539-79598682 | Common:8; Rare:34 | ||||
chr16:79770327-79770433 | Common:2; Rare:33 | ||||
chr16:85523262-85523406 | Common:3; Rare:31 | ||||
chr16:87924472-87924715 | Rare:63 | ||||
chr17:200302-200531 | Common:4; Rare:44 | ||||
chr17:321100-321443 | Common:3; Rare:112 | ||||
chr17:4497676-4497883 | Common:2; Rare:46 | ||||
chr17:5004300-5004583 | Rare:75; Clinvar (benign):1 | ||||
chr17:5500030-5500125 | Rare:18 | ||||
chr17:5500437-5500502 | Rare:13 | ||||
chr17:5530258-5530533 | Common:1; Rare:69 | ||||
chr17:7885875-7886266 | Common:5; Rare:85 | ||||
chr17:7887507-7887821 | Rare:71 | ||||
chr17:8484185-8484334 | Rare:52 | ||||
chr17:10406272-10406624 | Common:2; Rare:78; Clinvar (benign):1 |