Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:28742382-28742679 | Common:1; Rare:75 | ||||
chr22:28800535-28800702 | Common:4; Rare:63 | ||||
chr22:29267707-29268346 | Common:3; Rare:179 | ||||
chr22:29388480-29388700 | Rare:74 | ||||
chr22:29553547-29553848 | Rare:97 | ||||
chr22:29581074-29581247 | Common:3; Rare:49 | ||||
chr22:29766935-29767410 | Common:5; Rare:135 | ||||
chr22:29838193-29838322 | Common:3; Rare:52 | ||||
chr22:29882983-29883244 | Common:2; Rare:69 | ||||
chr22:30326861-30327194 | Common:2; Rare:116 | ||||
chr22:30356812-30357048 | Common:2; Rare:76 | ||||
chr22:30357435-30357458 | Rare:6 | ||||
chr22:30579900-30580106 | Rare:55 | ||||
chr22:30606587-30606859 | Common:3; Rare:60 | ||||
chr22:30607116-30607209 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |