Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77707991-77708207 | Common:2; Rare:109 | ||||
chr14:81220489-81220671 | Common:2; Rare:50 | ||||
chr14:81220871-81221069 | Common:1; Rare:94 | ||||
chr14:81221285-81221471 | Common:1; Rare:48 | ||||
chr14:81436403-81436605 | Common:3; Rare:77 | ||||
chr14:88562939-88563134 | Rare:91 | ||||
chr14:89619097-89619260 | Common:1; Rare:58 | ||||
chr14:89954689-89954956 | Rare:76 | ||||
chr14:90331906-90332203 | Common:1; Rare:86 | ||||
chr14:90396866-90397188 | Common:5; Rare:155 | ||||
chr14:90397205-90397233 | Rare:11 | ||||
chr14:91113850-91114132 | Rare:66 | ||||
chr14:91510254-91510624 | Common:1; Rare:116 | ||||
chr14:91836445-91836779 | Common:12; Rare:68 | ||||
chr14:92039843-92040187 | Common:3; Rare:93; Clinvar:6; Clinvar (benign):2 |