Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32014061-32014377 | Common:1; Rare:88 | ||||
chr1:32072764-32072993 | Rare:61 | ||||
chr1:32107968-32108118 | Rare:57 | ||||
chr1:32179627-32179771 | Rare:30 | ||||
chr1:32200495-32200709 | Rare:48 | ||||
chr1:32201585-32201702 | Rare:23 | ||||
chr1:32205505-32205699 | Common:1; Rare:78 | ||||
chr1:32291919-32292167 | Common:1; Rare:85 | ||||
chr1:32351410-32351639 | Common:1; Rare:60 | ||||
chr1:32394385-32394683 | Common:1; Rare:90 | ||||
chr1:32650918-32651318 | Common:2; Rare:150 | ||||
chr1:32702634-32702943 | Common:1; Rare:75 | ||||
chr1:32817257-32817674 | Rare:112; Clinvar:5 | ||||
chr1:33036800-33037155 | Rare:127; Clinvar (pathogenic):2 | ||||
chr1:33080994-33081196 | Common:1; Rare:60 |