Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58326875-58327018 | Common:1; Rare:30 | ||||
chr19:58499208-58499536 | Common:2; Rare:102; Clinvar:3 | ||||
chr2:677362-677557 | Common:1; Rare:82 | ||||
chr2:3558269-3558686 | Common:6; Rare:147 | ||||
chr2:3575122-3575358 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423451-9423697 | Rare:81 | ||||
chr2:9555818-9556057 | Rare:85 | ||||
chr2:17753764-17754125 | Common:3; Rare:116 | ||||
chr2:26244601-26244926 | Common:2; Rare:117; Clinvar:5; Clinvar (benign):6 | ||||
chr2:27212280-27212371 | Common:1; Rare:43 | ||||
chr2:27323067-27323209 | Common:2; Rare:46 | ||||
chr2:27356757-27357010 | Rare:60 | ||||
chr2:27370319-27370633 | Common:1; Rare:124 | ||||
chr2:27629014-27629054 | Common:1; Rare:18 | ||||
chr2:27663369-27663467 | Rare:28 |