Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7686128-7686783 | Rare:169 | ||||
chr17:7687463-7687640 | Rare:37 | ||||
chr17:7688116-7688492 | Common:5; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
chr17:7843591-7843762 | Rare:64 | ||||
chr17:7857170-7857296 | Common:1; Rare:69 | ||||
chr17:7857467-7857778 | Common:2; Rare:98 | ||||
chr17:7857868-7858322 | Common:2; Rare:161 | ||||
chr17:7884948-7885081 | Common:1; Rare:59 | ||||
chr17:7885187-7885355 | Rare:53 | ||||
chr17:7885523-7885621 | Rare:18 | ||||
chr17:7894210-7894443 | Rare:68 | ||||
chr17:7894663-7894936 | Rare:64 | ||||
chr17:7931852-7932300 | Common:5; Rare:123 | ||||
chr17:8118826-8119155 | Common:4; Rare:107 | ||||
chr17:8151158-8151507 | Common:3; Rare:85 |