Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75522378-75522582 | Rare:43 | ||||
chr14:75660845-75661003 | Rare:40 | ||||
chr14:75661180-75661340 | Common:2; Rare:47 | ||||
chr14:77320854-77321104 | Rare:77; Clinvar:1 | ||||
chr14:77377060-77377415 | Common:2; Rare:102 | ||||
chr14:77457536-77457884 | Common:1; Rare:104 | ||||
chr14:77457997-77458240 | Rare:57 | ||||
chr14:77707994-77708141 | Common:2; Rare:76 | ||||
chr14:89954640-89954938 | Rare:90 | ||||
chr14:89955817-89955984 | Common:8; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
chr14:92040035-92040181 | Common:2; Rare:38; Clinvar (benign):1 | ||||
chr14:92121658-92121979 | Common:4; Rare:108 | ||||
chr14:92122021-92122261 | Rare:64 | ||||
chr14:93184856-93185017 | Rare:53 | ||||
chr14:93185129-93185384 | Rare:72 |