Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:37748002-37748081 | Rare:35 | ||||
chr8:37749613-37749831 | Rare:41; Clinvar (pathogenic):1 | ||||
chr8:38148043-38148048 | |||||
chr8:38382982-38383074 | Rare:21 | ||||
chr8:38770169-38770184 | Rare:1 | ||||
chr8:47512224-47512578 | Rare:70 | ||||
chr8:47524508-47524529 | Rare:5 | ||||
chr8:47735156-47735186 | Rare:2 | ||||
chr8:47736226-47736421 | Rare:35 | ||||
chr8:47737260-47737773 | Common:3; Rare:169 | ||||
chr8:53483747-53483904 | Common:1; Rare:26 | ||||
chr8:58572111-58572290 | Rare:39 | ||||
chr8:96963188-96963428 | Common:1; Rare:35 | ||||
chr8:97065833-97066147 | Rare:79 | ||||
chr8:98030294-98030517 | Rare:39 |