Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:54162284-54162437 | Common:10; Rare:40 | ||||
chr19:54376084-54376143 | Rare:11 | ||||
chr19:55230508-55230678 | Common:3; Rare:81 | ||||
chr19:55240955-55241251 | Common:1; Rare:103 | ||||
chr19:56839775-56840059 | Common:1; Rare:72 | ||||
chr2:175825-176174 | Common:1; Rare:77 | ||||
chr2:180486-180646 | Rare:33 | ||||
chr2:289623-289832 | Rare:37 | ||||
chr2:289958-290033 | Common:1; Rare:15 | ||||
chr2:869323-869370 | Rare:11 | ||||
chr2:3604160-3604467 | Common:2; Rare:97; Clinvar (benign):1 | ||||
chr2:3626550-3626711 | Rare:39 | ||||
chr2:6918630-6918830 | Common:4; Rare:44 | ||||
chr2:9565615-9565686 | Common:1; Rare:11 | ||||
chr2:10036196-10036309 | Rare:17 |