Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69767687-69767822 | Common:1; Rare:69 | ||||
chr14:70416959-70417146 | Rare:57 | ||||
chr14:70641194-70641355 | Common:3; Rare:27 | ||||
chr14:72894074-72894260 | Common:4; Rare:63 | ||||
chr14:73058309-73058606 | Common:3; Rare:90 | ||||
chr14:73490742-73490959 | Rare:49 | ||||
chr14:73569104-73569292 | Rare:48 | ||||
chr14:73787129-73787372 | Common:2; Rare:87 | ||||
chr14:73950035-73950333 | Common:6; Rare:125; Clinvar (benign):5 | ||||
chr14:74019243-74019438 | Common:1; Rare:76 | ||||
chr14:74493275-74493795 | Common:4; Rare:167; Clinvar:2; Clinvar (benign):4 | ||||
chr14:74611611-74611785 | Rare:63; Clinvar:2 | ||||
chr14:74612189-74612374 | Rare:38 | ||||
chr14:74713058-74713218 | Rare:89 | ||||
chr14:75002741-75002982 | Common:1; Rare:79; Clinvar:2 |