Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:23889302-23889567 | Common:1; Rare:94 | ||||
chr13:24160572-24160764 | Rare:57 | ||||
chr13:24512739-24512843 | Common:3; Rare:31 | ||||
chr13:24922796-24923092 | Common:2; Rare:98; Clinvar:1 | ||||
chr13:25287372-25287609 | Common:2; Rare:71 | ||||
chr13:25301411-25301692 | Common:1; Rare:100 | ||||
chr13:25468679-25468996 | Common:1; Rare:109 | ||||
chr13:26221791-26221932 | Rare:35 | ||||
chr13:27251235-27251608 | Common:7; Rare:114 | ||||
chr13:27424514-27424711 | Common:2; Rare:64 | ||||
chr13:27450130-27450215 | Common:3; Rare:25 | ||||
chr13:28659071-28659187 | Rare:49; Clinvar (pathogenic):1 | ||||
chr13:30306974-30307221 | Common:5; Rare:63 | ||||
chr13:30307345-30307597 | Common:2; Rare:82 | ||||
chr13:30617255-30618052 | Common:1; Rare:243 |