Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43388310-43388676 | Common:11; Rare:65 | ||||
chr17:45247780-45247963 | Common:1; Rare:32 | ||||
chr17:47100277-47100376 | Rare:28 | ||||
chr17:48546477-48546680 | Rare:37 | ||||
chr17:48552881-48553033 | Rare:37 | ||||
chr17:48578345-48578622 | Common:3; Rare:66 | ||||
chr17:48598095-48598378 | Rare:59 | ||||
chr17:48961768-48961987 | Common:4; Rare:53 | ||||
chr17:48996485-48996598 | Common:1; Rare:25 | ||||
chr17:50151767-50151914 | Common:1; Rare:21 | ||||
chr17:50189857-50190356 | Common:2; Rare:145; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr17:50195048-50195137 | Common:1; Rare:16; Clinvar (benign):2 | ||||
chr17:50210361-50210613 | Common:2; Rare:65 | ||||
chr17:58324409-58324550 | Rare:44 | ||||
chr17:58631828-58632140 | Common:3; Rare:138 |