Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31703969-31704137 | Rare:35 | ||||
chr1:31938337-31938545 | Rare:66 | ||||
chr1:32013568-32013885 | Common:1; Rare:125 | ||||
chr1:32014539-32014731 | Rare:45 | ||||
chr1:32072936-32072993 | Rare:18 | ||||
chr1:32107957-32108130 | Rare:69 | ||||
chr1:32179621-32179768 | Rare:30 | ||||
chr1:32200532-32200654 | Rare:28 | ||||
chr1:32291821-32292302 | Common:1; Rare:133 | ||||
chr1:32331494-32331805 | Common:1; Rare:83 | ||||
chr1:32394418-32394705 | Common:1; Rare:79 | ||||
chr1:32650929-32651318 | Common:2; Rare:148 | ||||
chr1:32817281-32817686 | Rare:107; Clinvar:5; Clinvar (benign):1 | ||||
chr1:32895287-32895655 | Common:1; Rare:117 | ||||
chr1:32895658-32895984 | Common:1; Rare:105 |