Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3636241-3636737 | Common:7; Rare:135; Clinvar:5; Clinvar (benign):3 | ||||
chr17:3668565-3668822 | Common:2; Rare:101 | ||||
chr17:3723802-3723922 | Rare:66 | ||||
chr17:4142998-4143209 | Rare:71 | ||||
chr17:4263953-4264042 | Rare:37 | ||||
chr17:4704116-4704250 | Rare:74 | ||||
chr17:4939924-4940111 | Common:1; Rare:61 | ||||
chr17:5191833-5192077 | Common:1; Rare:80 | ||||
chr17:5420098-5420225 | Rare:51 | ||||
chr17:5486160-5486399 | Common:4; Rare:103 | ||||
chr17:6640646-6641044 | Common:6; Rare:107 | ||||
chr17:6651574-6651668 | Common:1; Rare:25 | ||||
chr17:7012315-7012675 | Rare:126 | ||||
chr17:7479517-7479709 | Common:1; Rare:31 | ||||
chr17:7484239-7484371 | Common:1; Rare:54 |