Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81220652-81221069 | Common:3; Rare:151 | ||||
chr14:81221274-81221554 | Common:1; Rare:87 | ||||
chr14:81436416-81436605 | Common:2; Rare:74 | ||||
chr14:85530024-85530213 | Common:1; Rare:40 | ||||
chr14:87992994-87993251 | Common:4; Rare:132; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
chr14:88562907-88563090 | Rare:85 | ||||
chr14:88792864-88793015 | Rare:51 | ||||
chr14:88824343-88824708 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
chr14:89416966-89417164 | Rare:57 | ||||
chr14:89494084-89494396 | Rare:47 | ||||
chr14:89619112-89619292 | Common:1; Rare:65 | ||||
chr14:89954640-89954935 | Rare:90 | ||||
chr14:89956440-89956556 | Common:1; Rare:29 | ||||
chr14:90256494-90256637 | Common:1; Rare:49 | ||||
chr14:90331900-90332411 | Common:1; Rare:131 |