Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81220871-81221069 | Common:1; Rare:94 | ||||
chr14:85530004-85530200 | Common:1; Rare:41 | ||||
chr14:85530334-85530497 | Rare:34 | ||||
chr14:88562933-88563126 | Rare:92 | ||||
chr14:88824411-88824708 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr14:89619119-89619307 | Common:1; Rare:67 | ||||
chr14:90396870-90397074 | Common:2; Rare:113 | ||||
chr14:91510260-91510606 | Common:1; Rare:108 | ||||
chr14:91836375-91836682 | Common:13; Rare:52 | ||||
chr14:92039832-92040192 | Common:3; Rare:96; Clinvar:6; Clinvar (benign):2 | ||||
chr14:92121636-92121990 | Common:5; Rare:118 | ||||
chr14:93184845-93185004 | Rare:51 | ||||
chr14:93206991-93207290 | Common:2; Rare:147 | ||||
chr14:94081133-94081341 | Common:4; Rare:69 | ||||
chr14:94390589-94390923 | Common:1; Rare:82 |