Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42050593-42050772 | Common:1; Rare:42 | ||||
chr17:42329428-42329644 | Common:1; Rare:55; Clinvar (benign):3 | ||||
chr17:42333746-42334015 | Rare:57; Clinvar:1 | ||||
chr17:43315632-43315916 | Common:6; Rare:120 | ||||
chr17:43388310-43388373 | Rare:12 | ||||
chr17:44207523-44207757 | Common:2; Rare:85 | ||||
chr17:45247795-45247975 | Common:1; Rare:31 | ||||
chr17:45585164-45585213 | Rare:3 | ||||
chr17:48728004-48728314 | Common:3; Rare:110; Clinvar:13; Clinvar (benign):12 | ||||
chr17:48728336-48728370 | Rare:12; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr17:48733159-48733436 | Common:2; Rare:60 | ||||
chr17:48734187-48734354 | Rare:35 | ||||
chr17:50062541-50062572 | Rare:2 | ||||
chr17:58324408-58324561 | Common:1; Rare:46 | ||||
chr17:59680746-59681026 | Rare:57 |