Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:90396870-90397222 | Common:5; Rare:167; Clinvar (benign):2 | ||||
chr14:91060164-91060393 | Common:3; Rare:90 | ||||
chr14:91060565-91060743 | Rare:61 | ||||
chr14:91114332-91114395 | Rare:10 | ||||
chr14:91244664-91244810 | Common:2; Rare:26 | ||||
chr14:91510230-91510631 | Common:1; Rare:130 | ||||
chr14:92039995-92040213 | Common:3; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92106554-92106751 | Common:2; Rare:64 | ||||
chr14:92121649-92122021 | Common:5; Rare:129 | ||||
chr14:92748555-92748819 | Rare:69 | ||||
chr14:92793994-92794408 | Rare:135 | ||||
chr14:92922992-92923153 | Common:3; Rare:40 | ||||
chr14:93115142-93115577 | Common:3; Rare:146 | ||||
chr14:93184822-93185017 | Rare:69 | ||||
chr14:93206985-93207288 | Common:2; Rare:147 |