Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48037610-48037789 | Common:1; Rare:81 | ||||
chr13:48233069-48233475 | Common:3; Rare:141 | ||||
chr13:48303684-48303907 | Rare:69; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48975792-48975928 | Common:1; Rare:50 | ||||
chr13:48976531-48976656 | Common:1; Rare:45 | ||||
chr13:49247807-49248092 | Rare:83 | ||||
chr13:49443997-49444476 | Common:1; Rare:156 | ||||
chr13:49585481-49585614 | Common:1; Rare:43 | ||||
chr13:49936222-49936586 | Common:1; Rare:112 | ||||
chr13:49996739-49997092 | Common:1; Rare:73 | ||||
chr13:50081992-50082262 | Common:1; Rare:78 | ||||
chr13:50715514-50715690 | Rare:34 | ||||
chr13:50909984-50910079 | Rare:25 | ||||
chr13:51452675-51452867 | Rare:48 | ||||
chr13:51453019-51453388 | Rare:143 |