Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:61711990-61712161 | Rare:26 | ||||
chr14:63229700-63229805 | Rare:16 | ||||
chr14:64080371-64080560 | Rare:58; Clinvar (benign):1 | ||||
chr14:64223076-64223273 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):3 | ||||
chr14:65468382-65468509 | Common:2; Rare:18 | ||||
chr14:67312341-67312651 | Common:2; Rare:71 | ||||
chr14:68792555-68792721 | Common:1; Rare:51 | ||||
chr14:73245963-73246135 | Common:2; Rare:78 | ||||
chr14:73713168-73713381 | Common:1; Rare:84 | ||||
chr14:74140317-74140598 | Rare:43 | ||||
chr14:74507285-74507571 | Rare:47 | ||||
chr14:75088618-75088892 | Common:2; Rare:53 | ||||
chr14:75277080-75277352 | Common:1; Rare:59 | ||||
chr14:75294193-75294451 | Common:1; Rare:71 | ||||
chr14:75426706-75426960 | Rare:44 |