Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1758804-1759061 | Common:1; Rare:66 | ||||
chr1:1778829-1778968 | Rare:38 | ||||
chr1:1890820-1891164 | Rare:124 | ||||
chr1:2391494-2391916 | Common:2; Rare:153 | ||||
chr1:2555752-2555847 | Rare:32 | ||||
chr1:2556072-2556410 | Common:2; Rare:117 | ||||
chr1:2556412-2556629 | Common:1; Rare:78 | ||||
chr1:2556984-2557278 | Common:3; Rare:63 | ||||
chr1:2586371-2586547 | Common:1; Rare:43 | ||||
chr1:3068764-3069050 | Common:2; Rare:77 | ||||
chr1:3069069-3069271 | Common:2; Rare:49; Clinvar (benign):2 | ||||
chr1:3624729-3625045 | Common:1; Rare:106 | ||||
chr1:3772482-3772774 | Common:3; Rare:59 | ||||
chr1:3857147-3857518 | Common:3; Rare:105 | ||||
chr1:3900174-3900422 | Common:12; Rare:117 |