Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7219817-7220036 | Common:4; Rare:93; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7222442-7222767 | Common:3; Rare:103; Clinvar:5; Clinvar (pathogenic):7 | ||||
chr17:7234472-7234668 | Common:2; Rare:103 | ||||
chr17:7241800-7241919 | Common:1; Rare:23 | ||||
chr17:7242240-7242618 | Common:1; Rare:113 | ||||
chr17:7251963-7252065 | Rare:42 | ||||
chr17:7315036-7315419 | Common:4; Rare:135 | ||||
chr17:7351626-7351733 | Rare:19 | ||||
chr17:7438162-7438317 | Common:1; Rare:33 | ||||
chr17:7484239-7484376 | Common:1; Rare:58 | ||||
chr17:7484503-7484834 | Common:2; Rare:130 | ||||
chr17:7561796-7561999 | Common:2; Rare:52 | ||||
chr17:7577054-7577487 | Common:1; Rare:104 | ||||
chr17:7583501-7583858 | Common:1; Rare:144; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7857504-7858003 | Common:4; Rare:155 |