Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74713078-74713194 | Rare:57 | ||||
chr14:75660875-75661368 | Common:5; Rare:118 | ||||
chr14:77320838-77321088 | Rare:77; Clinvar:1 | ||||
chr14:77457550-77457876 | Common:1; Rare:97 | ||||
chr14:77707979-77708117 | Rare:68 | ||||
chr14:85529893-85530184 | Common:2; Rare:61 | ||||
chr14:92121661-92121966 | Common:4; Rare:104 | ||||
chr14:92794004-92794398 | Rare:128 | ||||
chr14:93184886-93185008 | Rare:35 | ||||
chr14:93207121-93207288 | Common:2; Rare:77 | ||||
chr14:94081154-94081402 | Common:3; Rare:76 | ||||
chr14:95534730-95535058 | Common:4; Rare:100; Clinvar (benign):1 | ||||
chr14:96363311-96363550 | Common:1; Rare:80 | ||||
chr14:100376259-100376495 | Common:3; Rare:77 | ||||
chr14:102139729-102139919 | Rare:61 |