Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:5697396-5697633 | Common:1; Rare:57 | ||||
chr2:5981787-5982011 | Common:1; Rare:47 | ||||
chr2:6325490-6325812 | Common:1; Rare:59 | ||||
chr2:15941673-15941811 | Rare:39 | ||||
chr2:47335167-47335325 | Rare:33 | ||||
chr2:47798402-47798678 | Common:3; Rare:99; Clinvar:20; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
chr2:47906488-47906772 | Common:2; Rare:99 | ||||
chr2:58428006-58428369 | Common:1; Rare:90 | ||||
chr2:70086236-70086293 | Common:1; Rare:18 | ||||
chr2:70125262-70125483 | Rare:62 | ||||
chr2:74120555-74120650 | Common:1; Rare:24 | ||||
chr2:88016548-88016822 | Common:8; Rare:111 | ||||
chr2:91659922-91660011 | Rare:15 | ||||
chr2:95526713-95526818 | Common:1; Rare:37 | ||||
chr2:103295840-103295941 | Rare:15 |