Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:21140352-21140631 | Rare:125 | ||||
chr13:21176550-21176708 | Common:1; Rare:78 | ||||
chr13:24922810-24923039 | Common:1; Rare:71; Clinvar:1 | ||||
chr13:25301358-25301692 | Common:1; Rare:112 | ||||
chr13:26221791-26221924 | Rare:34 | ||||
chr13:27251258-27251605 | Common:3; Rare:101 | ||||
chr13:28138087-28138222 | Rare:46 | ||||
chr13:28658891-28659001 | Common:1; Rare:24 | ||||
chr13:28659076-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
chr13:28718813-28719123 | Common:1; Rare:78 | ||||
chr13:30306994-30307175 | Common:4; Rare:41 | ||||
chr13:30617294-30617375 | Rare:15 | ||||
chr13:30617588-30618034 | Common:1; Rare:136 | ||||
chr13:32031496-32031648 | Rare:28 | ||||
chr13:33285677-33285938 | Common:1; Rare:58 |