Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7394495-7394761 | Common:3; Rare:78 | ||||
chr17:7394827-7394991 | Rare:30 | ||||
chr17:7403747-7403903 | Common:5; Rare:40 | ||||
chr17:7404013-7404405 | Common:1; Rare:117 | ||||
chr17:7404889-7404950 | Rare:13 | ||||
chr17:7435364-7435564 | Common:2; Rare:39 | ||||
chr17:7435761-7435904 | Common:1; Rare:32 | ||||
chr17:7440043-7440204 | Rare:29 | ||||
chr17:7440332-7440411 | Rare:14 | ||||
chr17:7440927-7441019 | Common:1; Rare:17 | ||||
chr17:7455462-7455659 | Common:3; Rare:53; Clinvar (benign):2 | ||||
chr17:7455759-7456008 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:7479669-7479821 | Common:4; Rare:31 | ||||
chr17:7483790-7484039 | Common:6; Rare:61 | ||||
chr17:7484148-7485073 | Common:4; Rare:368 |