Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154870263-154870448 | Rare:38 | ||||
chr1:154936493-154936754 | Common:2; Rare:74 | ||||
chr1:154936842-154937377 | Common:1; Rare:124 | ||||
chr1:154956090-154956239 | Common:1; Rare:43 | ||||
chr1:154961704-154961883 | Common:1; Rare:73 | ||||
chr1:154961910-154962140 | Rare:64 | ||||
chr1:154970674-154970889 | Common:1; Rare:40 | ||||
chr1:154973700-154973972 | Rare:73 | ||||
chr1:154974315-154974695 | Rare:88 | ||||
chr1:154974877-154975160 | Common:3; Rare:97 | ||||
chr1:154975208-154975312 | Rare:15 | ||||
chr1:154983051-154983457 | Common:2; Rare:84; Clinvar (benign):2 | ||||
chr1:155002097-155002376 | Common:1; Rare:79 | ||||
chr1:155002518-155002680 | Common:1; Rare:14 | ||||
chr1:155003281-155003485 | Common:3; Rare:44 |