Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75522378-75522520 | Rare:30 | ||||
chr14:75661154-75661326 | Common:2; Rare:45 | ||||
chr14:77320854-77321051 | Rare:59; Clinvar:1 | ||||
chr14:77457559-77457877 | Common:1; Rare:94 | ||||
chr14:77458003-77458103 | Rare:24 | ||||
chr14:77707989-77708125 | Rare:67 | ||||
chr14:81220611-81220633 | Rare:2 | ||||
chr14:88005041-88005195 | Rare:24 | ||||
chr14:89954711-89954970 | Rare:70 | ||||
chr14:89955814-89955964 | Common:9; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr14:91113859-91114112 | Rare:58 | ||||
chr14:91510205-91510344 | Rare:56 | ||||
chr14:92121661-92121735 | Rare:39 | ||||
chr14:92651305-92651652 | Common:2; Rare:82 | ||||
chr14:93184851-93185022 | Rare:60 |