Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69399097-69399244 | Rare:22 | ||||
chr14:69611379-69611781 | Common:1; Rare:140 | ||||
chr14:70359528-70359804 | Common:1; Rare:66 | ||||
chr14:70416981-70417131 | Rare:47 | ||||
chr14:71320325-71320503 | Rare:57 | ||||
chr14:71321332-71321426 | Common:2; Rare:33 | ||||
chr14:73058238-73058588 | Common:3; Rare:112 | ||||
chr14:73787125-73787316 | Common:1; Rare:70 | ||||
chr14:73851732-73851974 | Common:4; Rare:82 | ||||
chr14:73950130-73950333 | Common:4; Rare:87; Clinvar (benign):2 | ||||
chr14:74019230-74019496 | Common:1; Rare:98 | ||||
chr14:74493462-74493770 | Common:3; Rare:109; Clinvar (benign):4 | ||||
chr14:74713053-74713224 | Rare:93 | ||||
chr14:75126994-75127132 | Rare:50 | ||||
chr14:75280368-75280533 | Common:1; Rare:27 |