Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:218346852-218347068 | Rare:58; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:219173717-219173975 | Common:2; Rare:135 | ||||
chr1:219210122-219210379 | Common:1; Rare:39 | ||||
chr1:220046345-220046643 | Common:1; Rare:110 | ||||
chr1:220093943-220094344 | Common:4; Rare:135; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:221742027-221742417 | Common:2; Rare:100 | ||||
chr1:222589765-222589850 | Rare:26 | ||||
chr1:222589855-222590226 | Common:3; Rare:83 | ||||
chr1:222712447-222712858 | Common:3; Rare:147 | ||||
chr1:222713254-222713642 | Rare:111 | ||||
chr1:223701373-223701613 | Common:1; Rare:31 | ||||
chr1:223769641-223769891 | Rare:54 | ||||
chr1:223845668-223845802 | Rare:53 | ||||
chr1:224183147-224183293 | Common:2; Rare:74 | ||||
chr1:224330120-224330442 | Common:7; Rare:98 |