Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:242025757-242026157 | Common:3; Rare:137 | ||||
chr1:242586333-242586733 | Common:16; Rare:185 | ||||
chr1:243316556-243316739 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr1:243346016-243346412 | Rare:69 | ||||
chr1:243713650-243714070 | Common:2; Rare:63 | ||||
chr1:243851906-243852306 | Common:5; Rare:124 | ||||
chr1:243903080-243903480 | Rare:109 | ||||
chr1:243968349-243968749 | Rare:121 | ||||
chr1:244011470-244012128 | Common:5; Rare:159 | ||||
chr1:244012195-244012423 | Rare:43 | ||||
chr1:244046893-244047752 | Common:7; Rare:222 | ||||
chr1:244049690-244050005 | Rare:79 | ||||
chr1:244053905-244054186 | Rare:52; Clinvar (pathogenic):2 | ||||
chr1:244056551-244056792 | Common:3; Rare:71 | ||||
chr1:244239440-244239800 | Common:2; Rare:65 |